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Links from MedGen

Items: 1 to 100 of 637

VariationLocationGene(s)Protein changeCondition(s)Clinical significance
(Last reviewed)		Review status
1.
GRCh37:
Chr11:76916578
GRCh38:
Chr11:77205533
MYO7AL1813P, L1802P, L1851PAutosomal recessive nonsyndromic hearing loss 2Likely pathogenic
(Feb 28, 2023)		criteria provided, single submitter
2.
GRCh37:
Chr11:76909626
GRCh38:
Chr11:77198581
MYO7AE1499K, E1510KAutosomal recessive nonsyndromic hearing loss 2Likely pathogenic
(Nov 10, 2022)		criteria provided, single submitter
3.
GRCh37:
Chr11:76900495-76900498
GRCh38:
Chr11:77189450-77189453
MYO7AS1194fs, S1205fsAutosomal recessive nonsyndromic hearing loss 2Likely pathogenic
(Nov 10, 2022)		criteria provided, single submitter
4.
GRCh37:
Chr11:76901884
GRCh38:
Chr11:77190839
MYO7AG1298E, G1287EAutosomal recessive nonsyndromic hearing loss 2Likely pathogenic
(Nov 10, 2022)		criteria provided, single submitter
5.
GRCh37:
Chr11:76873367
GRCh38:
Chr11:77162321
MYO7AK504N, K515Nnot provided, Autosomal recessive nonsyndromic hearing loss 2Conflicting interpretations of pathogenicity
(Feb 28, 2023)		criteria provided, conflicting interpretations
6.
GRCh37:
Chr11:76914188
GRCh38:
Chr11:77203143
MYO7AP1702L, P1713L, P1751Lnot provided, Autosomal dominant nonsyndromic hearing loss 11, Usher syndrome type 1,
Autosomal recessive nonsyndromic hearing loss 2		Uncertain significance
(Nov 30, 2021)		criteria provided, multiple submitters, no conflicts
7.
GRCh37:
Chr11:76916548
GRCh38:
Chr11:77205503
MYO7AT1792M, T1803M, T1841Mnot specified, not provided, Autosomal recessive nonsyndromic hearing loss 2,
Usher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11		Uncertain significance
(Apr 27, 2023)		criteria provided, multiple submitters, no conflicts
8.
GRCh37:
Chr11:76867804
GRCh38:
Chr11:77156758
MYO7AL190W, L179Wnot provided, Autosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2,
Usher syndrome type 1		Uncertain significance
(Nov 1, 2022)		criteria provided, multiple submitters, no conflicts
9.
GRCh37:
Chr11:76905543
GRCh38:
Chr11:77194498
MYO7AQ1422*, Q1433*Autosomal recessive nonsyndromic hearing loss 2Pathogenic
(Aug 1, 2020)		criteria provided, single submitter
10.
GRCh37:
Chr11:76891516
GRCh38:
Chr11:77180470
MYO7AR884C, R895Cnot provided, Usher syndrome type 1, not specified,
Autosomal recessive nonsyndromic hearing loss 2		Conflicting interpretations of pathogenicity
(May 4, 2023)		criteria provided, conflicting interpretations
11.
GRCh37:
Chr11:76922953
GRCh38:
Chr11:77211908
MYO7AT2060P, T2071P, T2109PAutosomal recessive nonsyndromic hearing loss 2Uncertain significanceno assertion criteria provided
12.
GRCh37:
Chr11:76918340
GRCh38:
Chr11:77207295
MYO7AE1868K, E1879K, E1917Knot provided, Autosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2,
Usher syndrome type 1		Uncertain significance
(Apr 12, 2022)		criteria provided, multiple submitters, no conflicts
13.
GRCh37:
Chr11:76877149-76877156
GRCh38:
Chr11:77166103-77166110
MYO7AV570fs, V581fsAutosomal recessive nonsyndromic hearing loss 2, not providedPathogenic/Likely pathogenic
(Nov 10, 2022)		criteria provided, multiple submitters, no conflicts
14.
GRCh37:
Chr11:76892528
GRCh38:
Chr11:77181482
MYO7AR922C, R933CAutosomal recessive nonsyndromic hearing loss 2, not provided, Usher syndrome type 1
Uncertain significance
(Apr 30, 2022)		criteria provided, multiple submitters, no conflicts
15.
GRCh37:
Chr11:76924930
GRCh38:
Chr11:77213885
MYO7AT2106I, T2115I, T2155IUsher syndrome type 1, Autosomal recessive nonsyndromic hearing loss 2Uncertain significance
(Jul 22, 2021)		criteria provided, single submitter
16.
GRCh37:
Chr11:76910722
GRCh38:
Chr11:77199677
MYO7AT1522S, T1533S, T1571SAutosomal recessive nonsyndromic hearing loss 2Uncertain significance
(Jul 22, 2021)		criteria provided, single submitter
17.
GRCh37:
Chr11:76901092
GRCh38:
Chr11:77190047
MYO7AP1209A, P1220AAutosomal recessive nonsyndromic hearing loss 2, Autosomal recessive nonsyndromic hearing loss 2, Usher syndrome type 1,
Autosomal dominant nonsyndromic hearing loss 11		Uncertain significance
(Jul 22, 2021)		criteria provided, multiple submitters, no conflicts
18.
GRCh37:
Chr11:76868432
GRCh38:
Chr11:77157386
MYO7Anot provided, Autosomal recessive nonsyndromic hearing loss 2, Usher syndrome type 1,
Autosomal dominant nonsyndromic hearing loss 11		Conflicting interpretations of pathogenicity
(Aug 19, 2022)		criteria provided, conflicting interpretations
19.
GRCh37:
Chr11:76858896
GRCh38:
Chr11:77147850
MYO7AT51M, T62MUsher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2
Uncertain significance
(Jul 14, 2021)		criteria provided, single submitter
20.
GRCh37:
Chr11:76901098
GRCh38:
Chr11:77190053
MYO7AG1211S, G1222SUsher syndrome type 1, Autosomal recessive nonsyndromic hearing loss 2, Autosomal dominant nonsyndromic hearing loss 11,
not provided		Uncertain significance
(Oct 19, 2021)		criteria provided, multiple submitters, no conflicts
21.
GRCh37:
Chr11:76874013
GRCh38:
Chr11:77162967
MYO7AI546V, I557VUsher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2
Uncertain significance
(Jul 14, 2021)		criteria provided, single submitter
22.
GRCh37:
Chr11:76890815
GRCh38:
Chr11:77179769
MYO7AH790P, H801PUsher syndrome type 1, Autosomal recessive nonsyndromic hearing loss 2, Usher syndrome type 1,
Autosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2, Autosomal dominant nonsyndromic hearing loss 11
Uncertain significance
(Oct 27, 2021)		criteria provided, multiple submitters, no conflicts
23.
GRCh37:
Chr11:76901816
GRCh38:
Chr11:77190771
MYO7Anot provided, Autosomal recessive nonsyndromic hearing loss 2, Usher syndrome type 1,
Autosomal dominant nonsyndromic hearing loss 11		Conflicting interpretations of pathogenicity
(Aug 6, 2022)		criteria provided, conflicting interpretations
24.
GRCh37:
Chr11:76871213-76871214
GRCh38:
Chr11:77160167-77160168
MYO7AD354fs, D365fsnot providedPathogenic
(Sep 23, 2022)		criteria provided, single submitter
25.
GRCh37:
Chr11:76924956
GRCh38:
Chr11:77213911
MYO7AN2115fs, N2124fs, N2164fsAutosomal recessive nonsyndromic hearing loss 2Likely pathogenicno assertion criteria provided
26.
GRCh37:
Chr11:76903309
GRCh38:
Chr11:77192264
MYO7AY1369H, Y1380HUsher syndromeLikely pathogenic
(Dec 31, 2022)		criteria provided, single submitter
27.
GRCh37:
Chr11:76885812
GRCh38:
Chr11:77174766
MYO7AR638Q, R649QAutosomal recessive nonsyndromic hearing loss 2Uncertain significance
(Jul 1, 2021)		no assertion criteria provided
28.
GRCh37:
Chr11:76874023
GRCh38:
Chr11:77162977
MYO7AY549C, Y560CUsher syndrome type 1, Usher syndromePathogenic/Likely pathogenic
(Dec 31, 2022)		criteria provided, multiple submitters, no conflicts
29.
GRCh37:
Chr11:76925011
GRCh38:
Chr11:77213966
MYO7AC2133S, C2142S, C2182SAutosomal recessive nonsyndromic hearing loss 2Uncertain significance
(Jul 1, 2021)		no assertion criteria provided
30.
GRCh37:
Chr11:76912683
GRCh38:
Chr11:77201638
MYO7AAutosomal recessive nonsyndromic hearing loss 2Uncertain significance
(Jul 1, 2021)		no assertion criteria provided
31.
GRCh37:
Chr11:76912612
GRCh38:
Chr11:77201567
MYO7AQ1609*, Q1620*, Q1658*not provided, Usher syndrome type 1Pathogenic/Likely pathogenic
(Jun 13, 2022)		criteria provided, multiple submitters, no conflicts
32.
GRCh37:
Chr11:76901876
GRCh38:
Chr11:77190831
MYO7AR1285fs, R1296fsAutosomal recessive nonsyndromic hearing loss 2Likely pathogenicno assertion criteria provided
33.
GRCh37:
Chr11:76908838
GRCh38:
Chr11:77197793
MYO7AAutosomal dominant nonsyndromic hearing loss 11, Usher syndrome type 1, Autosomal recessive nonsyndromic hearing loss 2
Benign
(Jul 1, 2021)		criteria provided, single submitter
34.
GRCh37:
Chr11:76908791
GRCh38:
Chr11:77197746
MYO7AUsher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2
Benign
(Jul 1, 2021)		criteria provided, single submitter
35.
GRCh37:
Chr11:76908732
GRCh38:
Chr11:77197687
MYO7AAutosomal dominant nonsyndromic hearing loss 11, Usher syndrome type 1, Autosomal recessive nonsyndromic hearing loss 2
Benign/Likely benign
(Jul 1, 2021)		criteria provided, single submitter
36.
GRCh37:
Chr11:76858756
GRCh38:
Chr11:77147710
MYO7AAutosomal dominant nonsyndromic hearing loss 11, Usher syndrome type 1, Autosomal recessive nonsyndromic hearing loss 2,
not provided		Benign
(Jul 1, 2021)		criteria provided, multiple submitters, no conflicts
37.
GRCh37:
Chr11:76923017
GRCh38:
Chr11:77211972
MYO7AUsher syndrome type 1, Autosomal recessive nonsyndromic hearing loss 2, Autosomal dominant nonsyndromic hearing loss 11,
not provided		Benign/Likely benign
(Jul 1, 2021)		criteria provided, multiple submitters, no conflicts
38.
GRCh37:
Chr11:76892835
GRCh38:
Chr11:77181789
MYO7AUsher syndrome type 1, Autosomal recessive nonsyndromic hearing loss 2, Autosomal dominant nonsyndromic hearing loss 11,
not provided		Benign
(Jul 1, 2021)		criteria provided, multiple submitters, no conflicts
39.
GRCh37:
Chr11:76890071
GRCh38:
Chr11:77179025
MYO7Anot provided, Autosomal recessive nonsyndromic hearing loss 2, Usher syndrome type 1,
Autosomal dominant nonsyndromic hearing loss 11		Benign/Likely benign
(Sep 6, 2022)		criteria provided, multiple submitters, no conflicts
40.
GRCh37:
Chr11:76901067
GRCh38:
Chr11:77190022
MYO7AUsher syndrome type 1, not provided, Autosomal recessive nonsyndromic hearing loss 2,
Autosomal dominant nonsyndromic hearing loss 11		Conflicting interpretations of pathogenicity
(Oct 19, 2022)		criteria provided, conflicting interpretations
41.
GRCh37:
Chr11:76910745
GRCh38:
Chr11:77199700
MYO7AAutosomal recessive nonsyndromic hearing loss 2, Autosomal dominant nonsyndromic hearing loss 11, Usher syndrome type 1,
not provided		Conflicting interpretations of pathogenicity
(Sep 22, 2022)		criteria provided, conflicting interpretations
42.
GRCh37:
Chr11:76922271
GRCh38:
Chr11:77211226
MYO7AY1993*, Y2004*, Y2042*not providedPathogenic
(Oct 15, 2020)		criteria provided, single submitter
43.
GRCh37:
Chr11:76903129
GRCh38:
Chr11:77192084
MYO7AM1309V, M1320VHearing impairment, Autosomal recessive nonsyndromic hearing loss 2, Autosomal dominant nonsyndromic hearing loss 11,
Usher syndrome type 1		Uncertain significance
(Jul 23, 2021)		criteria provided, multiple submitters, no conflicts
44.
GRCh37:
Chr11:76890844
GRCh38:
Chr11:77179798
MYO7AR800C, R811Cnot provided, Autosomal dominant nonsyndromic hearing loss 11, Usher syndrome type 1,
Autosomal recessive nonsyndromic hearing loss 2		Uncertain significance
(Jul 6, 2022)		criteria provided, multiple submitters, no conflicts
45.
GRCh37:
Chr11:76901793-76901796
GRCh38:
Chr11:77190748-77190751
MYO7AT1257fs, T1268fsAutosomal recessive nonsyndromic hearing loss 2Likely pathogenic
(Mar 21, 2018)		criteria provided, single submitter
46.
GRCh37:
Chr11:76913424
GRCh38:
Chr11:77202379
MYO7AR1659H, R1670H, R1708Hnot provided, Autosomal recessive nonsyndromic hearing loss 2Uncertain significance
(May 19, 2022)		criteria provided, multiple submitters, no conflicts
47.
GRCh37:
Chr11:76885949
GRCh38:
Chr11:77174903
MYO7AA684T, A695TAutosomal recessive nonsyndromic hearing loss 2, not providedUncertain significance
(May 18, 2021)		criteria provided, multiple submitters, no conflicts
48.
GRCh37:
Chr11:76883843
GRCh38:
Chr11:77172797
MYO7AR605Q, R616Qnot provided, Autosomal recessive nonsyndromic hearing loss 2Conflicting interpretations of pathogenicity
(Aug 13, 2022)		criteria provided, conflicting interpretations
49.
GRCh37:
Chr11:76871293
GRCh38:
Chr11:77160247
MYO7AE378K, E389KUsher syndrome type 1, Autosomal recessive nonsyndromic hearing loss 2, not provided
Uncertain significance
(Jan 13, 2022)		criteria provided, multiple submitters, no conflicts
50.
GRCh37:
Chr11:76912661
GRCh38:
Chr11:77201616
MYO7AT1625N, T1636N, T1674Nnot provided, Usher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11,
Autosomal recessive nonsyndromic hearing loss 2		Uncertain significance
(Jul 19, 2022)		criteria provided, multiple submitters, no conflicts
51.
GRCh37:
Chr11:76890174
GRCh38:
Chr11:77179128
MYO7AL778P, L789PUsher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2,
not provided		Uncertain significance
(Oct 25, 2022)		criteria provided, multiple submitters, no conflicts
52.
GRCh37:
Chr11:76853874
GRCh38:
Chr11:77142828
MYO7AUsher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2,
not provided		Uncertain significance
(Jul 19, 2022)		criteria provided, multiple submitters, no conflicts
53.
GRCh37:
Chr11:76892448
GRCh38:
Chr11:77181402
MYO7AR895H, R906Hnot provided, Usher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11,
Autosomal recessive nonsyndromic hearing loss 2		Uncertain significance
(Oct 5, 2022)		criteria provided, multiple submitters, no conflicts
54.
GRCh37:
Chr11:76912591
GRCh38:
Chr11:77201546
MYO7AG1602S, G1651S, G1613Snot provided, Autosomal recessive nonsyndromic hearing loss 2Pathogenic
(Aug 31, 2022)		criteria provided, multiple submitters, no conflicts
55.
GRCh37:
Chr11:76903174
GRCh38:
Chr11:77192129
MYO7AA1324T, A1335TUsher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2,
not provided		Uncertain significance
(Apr 15, 2022)		criteria provided, multiple submitters, no conflicts
56.
GRCh37:
Chr11:76924993
GRCh38:
Chr11:77213948
MYO7AR2176H, R2136H, R2127HUsher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2,
not provided		Uncertain significance
(Sep 27, 2022)		criteria provided, multiple submitters, no conflicts
57.
GRCh37:
Chr11:76867129
GRCh38:
Chr11:77156083
MYO7AC154*, C143*not provided, Autosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2,
Usher syndrome type 1		Pathogenic
(Jun 13, 2022)		criteria provided, multiple submitters, no conflicts
58.
GRCh37:
Chr11:76874037
GRCh38:
Chr11:77162991
MYO7AUsher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2,
not provided		Uncertain significance
(May 3, 2022)		criteria provided, multiple submitters, no conflicts
59.
GRCh37:
Chr11:76914236
GRCh38:
Chr11:77203191
MYO7AS1718L, S1729L, S1767LUsher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2,
Inborn genetic diseases, not provided		Uncertain significance
(Jul 30, 2022)		criteria provided, multiple submitters, no conflicts
60.
GRCh37:
Chr11:76867953
GRCh38:
Chr11:77156907
MYO7AF213Y, F202YAutosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2, Usher syndrome type 1,
not provided		Uncertain significance
(Oct 6, 2021)		criteria provided, multiple submitters, no conflicts
61.
GRCh37:
Chr11:76890880
GRCh38:
Chr11:77179834
MYO7AR812C, R823Cnot specified, not provided, Usher syndrome type 1,
Autosomal recessive nonsyndromic hearing loss 2, Autosomal dominant nonsyndromic hearing loss 11		Uncertain significance
(Dec 20, 2022)		criteria provided, multiple submitters, no conflicts
62.
GRCh37:
Chr11:76867061
GRCh38:
Chr11:77156015
MYO7AP121S, P132SUsher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2
Uncertain significance
(Jan 13, 2018)		criteria provided, single submitter
63.
GRCh37:
Chr11:76916615
GRCh38:
Chr11:77205570
MYO7AUsher syndrome type 1, not provided, Autosomal dominant nonsyndromic hearing loss 11,
Autosomal recessive nonsyndromic hearing loss 2		Conflicting interpretations of pathogenicity
(Jan 31, 2022)		criteria provided, conflicting interpretations
64.
GRCh37:
Chr11:76839530
GRCh38:
Chr11:77128484
MYO7AUsher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2
Uncertain significance
(Apr 27, 2017)		criteria provided, single submitter
65.
GRCh37:
Chr11:76912658
GRCh38:
Chr11:77201613
MYO7AV1624D, V1635D, V1673Dnot provided, Autosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2,
Usher syndrome type 1		Uncertain significance
(Sep 1, 2021)		criteria provided, multiple submitters, no conflicts
66.
GRCh37:
Chr11:76909574
GRCh38:
Chr11:77198529
MYO7AUsher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2,
not provided		Conflicting interpretations of pathogenicity
(Jun 25, 2022)		criteria provided, conflicting interpretations
67.
GRCh37:
Chr11:76894214
GRCh38:
Chr11:77183169
MYO7Anot provided, Usher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11,
Autosomal recessive nonsyndromic hearing loss 2		Conflicting interpretations of pathogenicity
(May 12, 2022)		criteria provided, conflicting interpretations
68.
GRCh37:
Chr11:76891431
GRCh38:
Chr11:77180385
MYO7Anot specified, Usher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11,
Autosomal recessive nonsyndromic hearing loss 2, not provided		Conflicting interpretations of pathogenicity
(Aug 15, 2022)		criteria provided, conflicting interpretations
69.
GRCh37:
Chr11:76885836
GRCh38:
Chr11:77174790
MYO7AR646Q, R657QUsher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2,
not provided		Conflicting interpretations of pathogenicity
(Oct 13, 2022)		criteria provided, conflicting interpretations
70.
GRCh37:
Chr11:76874038
GRCh38:
Chr11:77162992
MYO7AUsher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2
Uncertain significance
(Apr 27, 2017)		criteria provided, single submitter
71.
GRCh37:
Chr11:76922256
GRCh38:
Chr11:77211211
MYO7AUsher syndrome type 1, not provided, Autosomal recessive nonsyndromic hearing loss 2,
Autosomal dominant nonsyndromic hearing loss 11		Conflicting interpretations of pathogenicity
(Sep 14, 2022)		criteria provided, conflicting interpretations
72.
GRCh37:
Chr11:76914122
GRCh38:
Chr11:77203077
MYO7AT1729M, T1691M, T1680MUsher syndrome type 1, not provided, Autosomal dominant nonsyndromic hearing loss 11,
Autosomal recessive nonsyndromic hearing loss 2		Uncertain significance
(Jul 5, 2022)		criteria provided, multiple submitters, no conflicts
73.
GRCh37:
Chr11:76910700
GRCh38:
Chr11:77199655
MYO7AUsher syndrome type 1, not provided, Autosomal dominant nonsyndromic hearing loss 11,
Autosomal recessive nonsyndromic hearing loss 2		Conflicting interpretations of pathogenicity
(Aug 23, 2022)		criteria provided, conflicting interpretations
74.
GRCh37:
Chr11:76908634
GRCh38:
Chr11:77197589
MYO7AK1478Q, K1467QUsher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2
Uncertain significance
(Jan 13, 2018)		criteria provided, single submitter
75.
GRCh37:
Chr11:76892518
GRCh38:
Chr11:77181472
MYO7AM918I, M929IUsher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2
Uncertain significance
(Jan 12, 2018)		criteria provided, single submitter
76.
GRCh37:
Chr11:76885808
GRCh38:
Chr11:77174762
MYO7AD637N, D648NUsher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11, not provided,
Autosomal recessive nonsyndromic hearing loss 2		Uncertain significance
(Jun 27, 2022)		criteria provided, multiple submitters, no conflicts
77.
GRCh37:
Chr11:76883867
GRCh38:
Chr11:77172821
MYO7AT613M, T624MAutosomal recessive nonsyndromic hearing loss 2, Usher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11,
Autosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2, not provided,
Usher syndrome type 1		Uncertain significance
(May 10, 2022)		criteria provided, multiple submitters, no conflicts
78.
GRCh37:
Chr11:76925942
GRCh38:
Chr11:77214897
MYO7AUsher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2
Uncertain significance
(Jan 12, 2018)		criteria provided, single submitter
79.
GRCh37:
Chr11:76924978
GRCh38:
Chr11:77213933
MYO7AI2122T, I2171T, I2131TUsher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2
Uncertain significance
(Jan 13, 2018)		criteria provided, single submitter
80.
GRCh37:
Chr11:76872007
GRCh38:
Chr11:77160961
MYO7Anot provided, Usher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11,
Autosomal recessive nonsyndromic hearing loss 2		Conflicting interpretations of pathogenicity
(Oct 24, 2022)		criteria provided, conflicting interpretations
81.
GRCh37:
Chr11:76868402
GRCh38:
Chr11:77157356
MYO7Anot provided, Autosomal recessive nonsyndromic hearing loss 2, Autosomal dominant nonsyndromic hearing loss 11,
Usher syndrome type 1		Conflicting interpretations of pathogenicity
(Jul 21, 2021)		criteria provided, conflicting interpretations
82.
GRCh37:
Chr11:76919760
GRCh38:
Chr11:77208715
MYO7AT1988I, T1939I, T1950IUsher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2
Uncertain significance
(Jan 13, 2018)		criteria provided, single submitter
83.
GRCh37:
Chr11:76919733
GRCh38:
Chr11:77208688
MYO7AUsher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2
Uncertain significance
(Jan 12, 2018)		criteria provided, single submitter
84.
GRCh37:
Chr11:76868330
GRCh38:
Chr11:77157284
MYO7AUsher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2
Uncertain significance
(Jan 13, 2018)		criteria provided, single submitter
85.
GRCh37:
Chr11:76867730
GRCh38:
Chr11:77156684
MYO7Anot provided, Usher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11,
Autosomal recessive nonsyndromic hearing loss 2		Conflicting interpretations of pathogenicity
(Aug 31, 2022)		criteria provided, conflicting interpretations
86.
GRCh37:
Chr11:76915191
GRCh38:
Chr11:77204146
MYO7AUsher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11, not provided,
Autosomal recessive nonsyndromic hearing loss 2		Conflicting interpretations of pathogenicity
(Jul 13, 2020)		criteria provided, conflicting interpretations
87.
GRCh37:
Chr11:76903299
GRCh38:
Chr11:77192254
MYO7AK1376N, K1365NUsher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2,
not provided		Uncertain significance
(Aug 27, 2021)		criteria provided, multiple submitters, no conflicts
88.
GRCh37:
Chr11:76901853
GRCh38:
Chr11:77190808
MYO7AA1288S, A1277SAutosomal recessive nonsyndromic hearing loss 2, Usher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11
Uncertain significance
(Jan 12, 2018)		criteria provided, single submitter
89.
GRCh37:
Chr11:76901072
GRCh38:
Chr11:77190027
MYO7AR1202Q, R1213Qnot provided, Usher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11,
Autosomal recessive nonsyndromic hearing loss 2		Uncertain significance
(Jun 1, 2022)		criteria provided, multiple submitters, no conflicts
90.
GRCh37:
Chr11:76893454
GRCh38:
Chr11:77182409
MYO7AUsher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2
Uncertain significance
(Jan 13, 2018)		criteria provided, single submitter
91.
GRCh37:
Chr11:76892486
GRCh38:
Chr11:77181440
MYO7AA908T, A919TAutosomal recessive nonsyndromic hearing loss 2, Autosomal dominant nonsyndromic hearing loss 11, not provided,
Usher syndrome type 1		Conflicting interpretations of pathogenicity
(Oct 25, 2022)		criteria provided, conflicting interpretations
92.
GRCh37:
Chr11:76926181
GRCh38:
Chr11:77215136
MYO7AUsher syndrome type 1, Autosomal recessive nonsyndromic hearing loss 2, Autosomal dominant nonsyndromic hearing loss 11
Uncertain significance
(Jan 13, 2018)		criteria provided, single submitter
93.
GRCh37:
Chr11:76926157
GRCh38:
Chr11:77215112
MYO7AUsher syndrome type 1, Autosomal recessive nonsyndromic hearing loss 2, Autosomal dominant nonsyndromic hearing loss 11
Conflicting interpretations of pathogenicity
(Jan 12, 2018)		criteria provided, conflicting interpretations
94.
GRCh37:
Chr11:76925841
GRCh38:
Chr11:77214796
MYO7AUsher syndrome type 1, Autosomal recessive nonsyndromic hearing loss 2, Autosomal dominant nonsyndromic hearing loss 11
Uncertain significance
(Jan 12, 2018)		criteria provided, single submitter
95.
GRCh37:
Chr11:76925816
GRCh38:
Chr11:77214771
MYO7AUsher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2
Uncertain significance
(Jan 12, 2018)		criteria provided, single submitter
96.
GRCh37:
Chr11:76925779
GRCh38:
Chr11:77214734
MYO7AUsher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2
Conflicting interpretations of pathogenicity
(Jan 12, 2018)		criteria provided, conflicting interpretations
97.
GRCh37:
Chr11:76903222
GRCh38:
Chr11:77192177
MYO7AF1340L, F1351Lnot provided, Usher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11,
Autosomal recessive nonsyndromic hearing loss 2		Uncertain significance
(Sep 18, 2022)		criteria provided, multiple submitters, no conflicts
98.
GRCh37:
Chr11:76901728
GRCh38:
Chr11:77190683
MYO7AUsher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2
Uncertain significance
(Jan 12, 2018)		criteria provided, single submitter
99.
GRCh37:
Chr11:76900479
GRCh38:
Chr11:77189434
MYO7AUsher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2,
not provided		Conflicting interpretations of pathogenicity
(Aug 20, 2022)		criteria provided, conflicting interpretations
100.
GRCh37:
Chr11:76893182
GRCh38:
Chr11:77182136
MYO7AD1019E, D1030EUsher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2
Uncertain significance
(Jan 13, 2018)		criteria provided, single submitter
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