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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs10000037

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr4:38922709 (GRCh38.p14) Help

The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.

Alleles
G>A
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.201625 (53368/264690, TOPMED)
A=0.237900 (36119/151824, ALFA)
A=0.203109 (28447/140058, GnomAD) (+ 18 more)
A=0.05131 (1450/28258, 14KJPN)
A=0.05084 (852/16760, 8.3KJPN)
A=0.1547 (991/6404, 1000G_30x)
A=0.1528 (765/5008, 1000G)
A=0.2199 (985/4480, Estonian)
A=0.2680 (1033/3854, ALSPAC)
A=0.2503 (928/3708, TWINSUK)
A=0.0496 (145/2922, KOREAN)
A=0.1561 (294/1884, HapMap)
A=0.254 (253/998, GoNL)
A=0.157 (98/626, Chileans)
A=0.252 (151/600, NorthernSweden)
A=0.236 (126/534, MGP)
A=0.227 (49/216, Qatari)
A=0.037 (8/216, Vietnamese)
G=0.463 (87/188, SGDP_PRJ)
A=0.30 (12/40, GENOME_DK)
G=0.45 (9/20, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
FAM114A1 : Intron Variant
Publications
0 citations
Genomic View
See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20230706150541
Population Group Sample Size Ref Allele Alt Allele
Total Global 151824 G=0.762100 A=0.237900
European Sub 131448 G=0.753385 A=0.246615
African Sub 7368 G=0.8191 A=0.1809
African Others Sub 254 G=0.803 A=0.197
African American Sub 7114 G=0.8197 A=0.1803
Asian Sub 678 G=0.931 A=0.069
East Asian Sub 514 G=0.940 A=0.060
Other Asian Sub 164 G=0.902 A=0.098
Latin American 1 Sub 838 G=0.788 A=0.212
Latin American 2 Sub 4422 G=0.8449 A=0.1551
South Asian Sub 196 G=0.857 A=0.143
Other Sub 6874 G=0.7920 A=0.2080


Help

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

Download
Study Population Group Sample Size Ref Allele Alt Allele
TopMed Global Study-wide 264690 G=0.798375 A=0.201625
Allele Frequency Aggregator Total Global 151824 G=0.762100 A=0.237900
Allele Frequency Aggregator European Sub 131448 G=0.753385 A=0.246615
Allele Frequency Aggregator African Sub 7368 G=0.8191 A=0.1809
Allele Frequency Aggregator Other Sub 6874 G=0.7920 A=0.2080
Allele Frequency Aggregator Latin American 2 Sub 4422 G=0.8449 A=0.1551
Allele Frequency Aggregator Latin American 1 Sub 838 G=0.788 A=0.212
Allele Frequency Aggregator Asian Sub 678 G=0.931 A=0.069
Allele Frequency Aggregator South Asian Sub 196 G=0.857 A=0.143
gnomAD - Genomes Global Study-wide 140058 G=0.796891 A=0.203109
gnomAD - Genomes European Sub 75858 G=0.76573 A=0.23427
gnomAD - Genomes African Sub 41958 G=0.82533 A=0.17467
gnomAD - Genomes American Sub 13642 G=0.84511 A=0.15489
gnomAD - Genomes Ashkenazi Jewish Sub 3322 G=0.8200 A=0.1800
gnomAD - Genomes East Asian Sub 3128 G=0.9367 A=0.0633
gnomAD - Genomes Other Sub 2150 G=0.7963 A=0.2037
14KJPN JAPANESE Study-wide 28258 G=0.94869 A=0.05131
8.3KJPN JAPANESE Study-wide 16760 G=0.94916 A=0.05084
1000Genomes_30x Global Study-wide 6404 G=0.8453 A=0.1547
1000Genomes_30x African Sub 1786 G=0.8438 A=0.1562
1000Genomes_30x Europe Sub 1266 G=0.7622 A=0.2378
1000Genomes_30x South Asian Sub 1202 G=0.8369 A=0.1631
1000Genomes_30x East Asian Sub 1170 G=0.9359 A=0.0641
1000Genomes_30x American Sub 980 G=0.857 A=0.143
1000Genomes Global Study-wide 5008 G=0.8472 A=0.1528
1000Genomes African Sub 1322 G=0.8404 A=0.1596
1000Genomes East Asian Sub 1008 G=0.9425 A=0.0575
1000Genomes Europe Sub 1006 G=0.7684 A=0.2316
1000Genomes South Asian Sub 978 G=0.828 A=0.172
1000Genomes American Sub 694 G=0.863 A=0.137
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.7801 A=0.2199
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.7320 A=0.2680
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.7497 A=0.2503
KOREAN population from KRGDB KOREAN Study-wide 2922 G=0.9504 A=0.0496
HapMap Global Study-wide 1884 G=0.8439 A=0.1561
HapMap American Sub 766 G=0.851 A=0.149
HapMap African Sub 690 G=0.814 A=0.186
HapMap Asian Sub 252 G=0.964 A=0.036
HapMap Europe Sub 176 G=0.756 A=0.244
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.746 A=0.254
Chileans Chilean Study-wide 626 G=0.843 A=0.157
Northern Sweden ACPOP Study-wide 600 G=0.748 A=0.252
Medical Genome Project healthy controls from Spanish population Spanish controls Study-wide 534 G=0.764 A=0.236
Qatari Global Study-wide 216 G=0.773 A=0.227
A Vietnamese Genetic Variation Database Global Study-wide 216 G=0.963 A=0.037
SGDP_PRJ Global Study-wide 188 G=0.463 A=0.537
The Danish reference pan genome Danish Study-wide 40 G=0.70 A=0.30
Siberian Global Study-wide 20 G=0.45 A=0.55
Help

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements
Sequence name Change
GRCh38.p14 chr 4 NC_000004.12:g.38922709G>A
GRCh37.p13 chr 4 NC_000004.11:g.38924330G>A
FAM114A1 RefSeqGene NG_053162.1:g.60033G>A
Gene: FAM114A1, family with sequence similarity 114 member A1 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
FAM114A1 transcript variant 2 NM_001330764.2:c.325-61G>A N/A Intron Variant
FAM114A1 transcript variant 4 NM_001350631.2:c.325-61G>A N/A Intron Variant
FAM114A1 transcript variant 5 NM_001350632.2:c.940-61G>A N/A Intron Variant
FAM114A1 transcript variant 6 NM_001350633.2:c.565-61G>A N/A Intron Variant
FAM114A1 transcript variant 7 NM_001350634.2:c.352-61G>A N/A Intron Variant
FAM114A1 transcript variant 8 NM_001350635.3:c.946-61G>A N/A Intron Variant
FAM114A1 transcript variant 9 NM_001375792.1:c.946-61G>A N/A Intron Variant
FAM114A1 transcript variant 10 NM_001375793.1:c.946-61G>A N/A Intron Variant
FAM114A1 transcript variant 1 NM_138389.4:c.946-61G>A N/A Intron Variant
FAM114A1 transcript variant 3 NR_033290.2:n. N/A Intron Variant
FAM114A1 transcript variant X1 XM_047416412.1:c.325-61G>A N/A Intron Variant
Help

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar
Help

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement G= A
GRCh38.p14 chr 4 NC_000004.12:g.38922709= NC_000004.12:g.38922709G>A
GRCh37.p13 chr 4 NC_000004.11:g.38924330= NC_000004.11:g.38924330G>A
FAM114A1 RefSeqGene NG_053162.1:g.60033= NG_053162.1:g.60033G>A
FAM114A1 transcript variant 2 NM_001330764.2:c.325-61= NM_001330764.2:c.325-61G>A
FAM114A1 transcript variant 4 NM_001350631.2:c.325-61= NM_001350631.2:c.325-61G>A
FAM114A1 transcript variant 5 NM_001350632.2:c.940-61= NM_001350632.2:c.940-61G>A
FAM114A1 transcript variant 6 NM_001350633.2:c.565-61= NM_001350633.2:c.565-61G>A
FAM114A1 transcript variant 7 NM_001350634.2:c.352-61= NM_001350634.2:c.352-61G>A
FAM114A1 transcript variant 8 NM_001350635.3:c.946-61= NM_001350635.3:c.946-61G>A
FAM114A1 transcript variant 9 NM_001375792.1:c.946-61= NM_001375792.1:c.946-61G>A
FAM114A1 transcript variant 10 NM_001375793.1:c.946-61= NM_001375793.1:c.946-61G>A
FAM114A1 transcript variant 1 NM_138389.2:c.946-61= NM_138389.2:c.946-61G>A
FAM114A1 transcript variant 1 NM_138389.4:c.946-61= NM_138389.4:c.946-61G>A
FAM114A1 transcript variant X1 XM_005262672.1:c.946-61= XM_005262672.1:c.946-61G>A
FAM114A1 transcript variant X3 XM_005262673.1:c.946-61= XM_005262673.1:c.946-61G>A
FAM114A1 transcript variant X3 XM_005262674.1:c.325-61= XM_005262674.1:c.325-61G>A
FAM114A1 transcript variant X1 XM_047416412.1:c.325-61= XM_047416412.1:c.325-61G>A
Help

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

106 SubSNP, 21 Frequency submissions
No Submitter Submission ID Date (Build)
1 WI_SSAHASNP ss13845679 Dec 05, 2003 (119)
2 CSHL-HAPMAP ss19565893 Feb 27, 2004 (120)
3 PERLEGEN ss24652499 Sep 20, 2004 (123)
4 ABI ss44495472 Mar 15, 2006 (126)
5 ILLUMINA ss65747981 Oct 16, 2006 (127)
6 AFFY ss66288217 Nov 30, 2006 (127)
7 PERLEGEN ss68896912 May 17, 2007 (127)
8 ILLUMINA ss74887660 Dec 06, 2007 (129)
9 AFFY ss75950711 Dec 06, 2007 (129)
10 KRIBB_YJKIM ss82640928 Dec 15, 2007 (130)
11 ILLUMINA ss159849728 Dec 01, 2009 (131)
12 ENSEMBL ss161548646 Dec 01, 2009 (131)
13 ILLUMINA ss169483626 Jul 04, 2010 (132)
14 AFFY ss169573875 Jul 04, 2010 (132)
15 BUSHMAN ss198385074 Jul 04, 2010 (132)
16 1000GENOMES ss220868414 Jul 14, 2010 (132)
17 1000GENOMES ss232350842 Jul 14, 2010 (132)
18 1000GENOMES ss239653107 Jul 15, 2010 (132)
19 PJP ss293328356 May 09, 2011 (134)
20 ILLUMINA ss479152942 May 04, 2012 (137)
21 ILLUMINA ss479153634 May 04, 2012 (137)
22 ILLUMINA ss479465578 Sep 08, 2015 (146)
23 ILLUMINA ss484377053 May 04, 2012 (137)
24 ILLUMINA ss536563737 Sep 08, 2015 (146)
25 TISHKOFF ss557447736 Apr 25, 2013 (138)
26 SSMP ss651230456 Apr 25, 2013 (138)
27 ILLUMINA ss778343366 Sep 08, 2015 (146)
28 ILLUMINA ss782634822 Sep 08, 2015 (146)
29 ILLUMINA ss783604379 Sep 08, 2015 (146)
30 ILLUMINA ss831884884 Sep 08, 2015 (146)
31 ILLUMINA ss833797999 Sep 08, 2015 (146)
32 EVA-GONL ss979998399 Aug 21, 2014 (142)
33 JMKIDD_LAB ss1071452040 Aug 21, 2014 (142)
34 1000GENOMES ss1309287480 Aug 21, 2014 (142)
35 DDI ss1429845038 Apr 01, 2015 (144)
36 EVA_GENOME_DK ss1580510090 Apr 01, 2015 (144)
37 EVA_DECODE ss1589492848 Apr 01, 2015 (144)
38 EVA_UK10K_ALSPAC ss1609864600 Apr 01, 2015 (144)
39 EVA_UK10K_TWINSUK ss1652858633 Apr 01, 2015 (144)
40 EVA_MGP ss1711056713 Apr 01, 2015 (144)
41 EVA_SVP ss1712666310 Apr 01, 2015 (144)
42 ILLUMINA ss1752521527 Sep 08, 2015 (146)
43 HAMMER_LAB ss1801298097 Sep 08, 2015 (146)
44 WEILL_CORNELL_DGM ss1923230219 Feb 12, 2016 (147)
45 JJLAB ss2022199049 Sep 14, 2016 (149)
46 USC_VALOUEV ss2150310250 Dec 20, 2016 (150)
47 HUMAN_LONGEVITY ss2262160756 Dec 20, 2016 (150)
48 SYSTEMSBIOZJU ss2625600082 Nov 08, 2017 (151)
49 ILLUMINA ss2634108012 Nov 08, 2017 (151)
50 GRF ss2705763938 Nov 08, 2017 (151)
51 GNOMAD ss2808000009 Nov 08, 2017 (151)
52 SWEGEN ss2994485102 Nov 08, 2017 (151)
53 BIOINF_KMB_FNS_UNIBA ss3024869554 Nov 08, 2017 (151)
54 CSHL ss3345650534 Nov 08, 2017 (151)
55 ILLUMINA ss3628945482 Oct 12, 2018 (152)
56 ILLUMINA ss3632045411 Oct 12, 2018 (152)
57 ILLUMINA ss3633332223 Oct 12, 2018 (152)
58 ILLUMINA ss3634051108 Oct 12, 2018 (152)
59 ILLUMINA ss3634948687 Oct 12, 2018 (152)
60 ILLUMINA ss3635734096 Oct 12, 2018 (152)
61 ILLUMINA ss3636651231 Oct 12, 2018 (152)
62 ILLUMINA ss3637486610 Oct 12, 2018 (152)
63 ILLUMINA ss3638481814 Oct 12, 2018 (152)
64 ILLUMINA ss3640655983 Oct 12, 2018 (152)
65 ILLUMINA ss3641161643 Oct 12, 2018 (152)
66 ILLUMINA ss3641458473 Oct 12, 2018 (152)
67 ILLUMINA ss3643433520 Oct 12, 2018 (152)
68 OMUKHERJEE_ADBS ss3646305696 Oct 12, 2018 (152)
69 EGCUT_WGS ss3662406004 Jul 13, 2019 (153)
70 EVA_DECODE ss3711831800 Jul 13, 2019 (153)
71 ACPOP ss3731052194 Jul 13, 2019 (153)
72 ILLUMINA ss3745248954 Jul 13, 2019 (153)
73 EVA ss3761668601 Jul 13, 2019 (153)
74 ILLUMINA ss3772743627 Jul 13, 2019 (153)
75 KHV_HUMAN_GENOMES ss3804800376 Jul 13, 2019 (153)
76 EVA ss3825655749 Apr 26, 2020 (154)
77 EVA ss3828483334 Apr 26, 2020 (154)
78 SGDP_PRJ ss3858675992 Apr 26, 2020 (154)
79 KRGDB ss3904850826 Apr 26, 2020 (154)
80 FSA-LAB ss3984281289 Apr 26, 2021 (155)
81 FSA-LAB ss3984281290 Apr 26, 2021 (155)
82 EVA ss3986277529 Apr 26, 2021 (155)
83 EVA ss4017141832 Apr 26, 2021 (155)
84 TOPMED ss4610055703 Apr 26, 2021 (155)
85 TOMMO_GENOMICS ss5165144134 Apr 26, 2021 (155)
86 1000G_HIGH_COVERAGE ss5258793191 Oct 13, 2022 (156)
87 EVA ss5314951489 Oct 13, 2022 (156)
88 EVA ss5348262985 Oct 13, 2022 (156)
89 HUGCELL_USP ss5457620072 Oct 13, 2022 (156)
90 EVA ss5507471447 Oct 13, 2022 (156)
91 1000G_HIGH_COVERAGE ss5539629036 Oct 13, 2022 (156)
92 EVA ss5623929067 Oct 13, 2022 (156)
93 EVA ss5624138432 Oct 13, 2022 (156)
94 SANFORD_IMAGENETICS ss5634786531 Oct 13, 2022 (156)
95 TOMMO_GENOMICS ss5699049471 Oct 13, 2022 (156)
96 EVA ss5799612867 Oct 13, 2022 (156)
97 EVA ss5800114560 Oct 13, 2022 (156)
98 YY_MCH ss5804953098 Oct 13, 2022 (156)
99 EVA ss5843843474 Oct 13, 2022 (156)
100 EVA ss5848606974 Oct 13, 2022 (156)
101 EVA ss5854176752 Oct 13, 2022 (156)
102 EVA ss5863007319 Oct 13, 2022 (156)
103 EVA ss5936524512 Oct 13, 2022 (156)
104 EVA ss5963179212 Oct 13, 2022 (156)
105 EVA ss5980217643 Oct 13, 2022 (156)
106 EVA ss5981221653 Oct 13, 2022 (156)
107 1000Genomes NC_000004.11 - 38924330 Oct 12, 2018 (152)
108 1000Genomes_30x NC_000004.12 - 38922709 Oct 13, 2022 (156)
109 The Avon Longitudinal Study of Parents and Children NC_000004.11 - 38924330 Oct 12, 2018 (152)
110 Chileans NC_000004.11 - 38924330 Apr 26, 2020 (154)
111 Genetic variation in the Estonian population NC_000004.11 - 38924330 Oct 12, 2018 (152)
112 The Danish reference pan genome NC_000004.11 - 38924330 Apr 26, 2020 (154)
113 gnomAD - Genomes NC_000004.12 - 38922709 Apr 26, 2021 (155)
114 Genome of the Netherlands Release 5 NC_000004.11 - 38924330 Apr 26, 2020 (154)
115 HapMap NC_000004.12 - 38922709 Apr 26, 2020 (154)
116 KOREAN population from KRGDB NC_000004.11 - 38924330 Apr 26, 2020 (154)
117 Medical Genome Project healthy controls from Spanish population NC_000004.11 - 38924330 Apr 26, 2020 (154)
118 Northern Sweden NC_000004.11 - 38924330 Jul 13, 2019 (153)
119 Qatari NC_000004.11 - 38924330 Apr 26, 2020 (154)
120 SGDP_PRJ NC_000004.11 - 38924330 Apr 26, 2020 (154)
121 Siberian NC_000004.11 - 38924330 Apr 26, 2020 (154)
122 8.3KJPN NC_000004.11 - 38924330 Apr 26, 2021 (155)
123 14KJPN NC_000004.12 - 38922709 Oct 13, 2022 (156)
124 TopMed NC_000004.12 - 38922709 Apr 26, 2021 (155)
125 UK 10K study - Twins NC_000004.11 - 38924330 Oct 12, 2018 (152)
126 A Vietnamese Genetic Variation Database NC_000004.11 - 38924330 Jul 13, 2019 (153)
127 ALFA NC_000004.12 - 38922709 Apr 26, 2021 (155)
Help

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID History Updated (Build)
rs17501399 Oct 07, 2004 (123)
rs59671856 Feb 26, 2009 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss198385074, ss293328356, ss479152942, ss1589492848, ss1712666310, ss3643433520 NC_000004.10:38600724:G:A NC_000004.12:38922708:G:A (self)
20666746, 11515254, 313994, 8144252, 6675029, 5074066, 12028220, 172473, 4337059, 5272149, 10692972, 2826604, 23113441, 11515254, 2527831, ss220868414, ss232350842, ss239653107, ss479153634, ss479465578, ss484377053, ss536563737, ss557447736, ss651230456, ss778343366, ss782634822, ss783604379, ss831884884, ss833797999, ss979998399, ss1071452040, ss1309287480, ss1429845038, ss1580510090, ss1609864600, ss1652858633, ss1711056713, ss1752521527, ss1801298097, ss1923230219, ss2022199049, ss2150310250, ss2625600082, ss2634108012, ss2705763938, ss2808000009, ss2994485102, ss3345650534, ss3628945482, ss3632045411, ss3633332223, ss3634051108, ss3634948687, ss3635734096, ss3636651231, ss3637486610, ss3638481814, ss3640655983, ss3641161643, ss3641458473, ss3646305696, ss3662406004, ss3731052194, ss3745248954, ss3761668601, ss3772743627, ss3825655749, ss3828483334, ss3858675992, ss3904850826, ss3984281289, ss3984281290, ss3986277529, ss4017141832, ss5165144134, ss5314951489, ss5348262985, ss5507471447, ss5623929067, ss5624138432, ss5634786531, ss5799612867, ss5800114560, ss5843843474, ss5848606974, ss5936524512, ss5963179212, ss5980217643, ss5981221653 NC_000004.11:38924329:G:A NC_000004.12:38922708:G:A (self)
27154971, 146316152, 2597206, 32886575, 447433259, 3514537931, ss2262160756, ss3024869554, ss3711831800, ss3804800376, ss4610055703, ss5258793191, ss5457620072, ss5539629036, ss5699049471, ss5804953098, ss5854176752, ss5863007319 NC_000004.12:38922708:G:A NC_000004.12:38922708:G:A (self)
ss13845679, ss19565893 NT_016297.15:6072972:G:A NC_000004.12:38922708:G:A (self)
ss24652499, ss44495472, ss65747981, ss66288217, ss68896912, ss74887660, ss75950711, ss82640928, ss159849728, ss161548646, ss169483626, ss169573875 NT_016297.16:6083691:G:A NC_000004.12:38922708:G:A (self)
Help

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs10000037

Help

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:
Select flank length:

Genomic regions, transcripts, and products
Top Help

NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Software version is: 2.0.1.post761+d5e8e07