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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.

rs244411

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr5:110742779 (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
C>A / C>G / C>T
Variation Type
SNV Single Nucleotide Variation
Frequency
C=0.161714 (42804/264690, TOPMED)
C=0.101663 (15259/150094, ALFA)
C=0.08196 (2316/28258, 14KJPN) (+ 17 more)
C=0.08025 (1345/16760, 8.3KJPN)
C=0.1519 (973/6404, 1000G_30x)
C=0.0935 (419/4480, Estonian)
C=0.0900 (347/3854, ALSPAC)
C=0.0920 (341/3708, TWINSUK)
C=0.0863 (253/2930, KOREAN)
C=0.1305 (272/2084, HGDP_Stanford)
C=0.1808 (342/1892, HapMap)
C=0.0862 (158/1832, Korea1K)
C=0.082 (82/998, GoNL)
C=0.113 (68/600, NorthernSweden)
C=0.095 (51/538, SGDP_PRJ)
C=0.171 (37/216, Qatari)
C=0.098 (21/214, Vietnamese)
C=0.04 (2/56, Ancient Sardinia)
C=0.04 (2/56, Siberian)
C=0.10 (4/40, GENOME_DK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
SLC25A46 : 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 150094 C=0.101663 G=0.000000, T=0.898337
European Sub 136698 C=0.096805 G=0.000000, T=0.903195
African Sub 2490 C=0.3245 G=0.0000, T=0.6755
African Others Sub 102 C=0.363 G=0.000, T=0.637
African American Sub 2388 C=0.3229 G=0.0000, T=0.6771
Asian Sub 262 C=0.107 G=0.000, T=0.893
East Asian Sub 180 C=0.100 G=0.000, T=0.900
Other Asian Sub 82 C=0.12 G=0.00, T=0.88
Latin American 1 Sub 276 C=0.214 G=0.000, T=0.786
Latin American 2 Sub 1992 C=0.1431 G=0.0000, T=0.8569
South Asian Sub 4866 C=0.0826 G=0.0000, T=0.9174
Other Sub 3510 C=0.1265 G=0.0000, T=0.8735


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 C=0.161714 T=0.838286
Allele Frequency Aggregator Total Global 150094 C=0.101663 G=0.000000, T=0.898337
Allele Frequency Aggregator European Sub 136698 C=0.096805 G=0.000000, T=0.903195
Allele Frequency Aggregator South Asian Sub 4866 C=0.0826 G=0.0000, T=0.9174
Allele Frequency Aggregator Other Sub 3510 C=0.1265 G=0.0000, T=0.8735
Allele Frequency Aggregator African Sub 2490 C=0.3245 G=0.0000, T=0.6755
Allele Frequency Aggregator Latin American 2 Sub 1992 C=0.1431 G=0.0000, T=0.8569
Allele Frequency Aggregator Latin American 1 Sub 276 C=0.214 G=0.000, T=0.786
Allele Frequency Aggregator Asian Sub 262 C=0.107 G=0.000, T=0.893
14KJPN JAPANESE Study-wide 28258 C=0.08196 T=0.91804
8.3KJPN JAPANESE Study-wide 16760 C=0.08025 T=0.91975
1000Genomes_30x Global Study-wide 6404 C=0.1519 T=0.8481
1000Genomes_30x African Sub 1786 C=0.2990 T=0.7010
1000Genomes_30x Europe Sub 1266 C=0.0900 T=0.9100
1000Genomes_30x South Asian Sub 1202 C=0.0857 T=0.9143
1000Genomes_30x East Asian Sub 1170 C=0.0829 T=0.9171
1000Genomes_30x American Sub 980 C=0.128 T=0.872
Genetic variation in the Estonian population Estonian Study-wide 4480 C=0.0935 T=0.9065
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 C=0.0900 T=0.9100
UK 10K study - Twins TWIN COHORT Study-wide 3708 C=0.0920 T=0.9080
KOREAN population from KRGDB KOREAN Study-wide 2930 C=0.0863 A=0.0000, G=0.0000, T=0.9137
HGDP-CEPH-db Supplement 1 Global Study-wide 2084 C=0.1305 T=0.8695
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 C=0.091 T=0.909
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 C=0.085 T=0.915
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 C=0.103 T=0.897
HGDP-CEPH-db Supplement 1 Europe Sub 320 C=0.075 T=0.925
HGDP-CEPH-db Supplement 1 Africa Sub 242 C=0.360 T=0.640
HGDP-CEPH-db Supplement 1 America Sub 216 C=0.162 T=0.838
HGDP-CEPH-db Supplement 1 Oceania Sub 72 C=0.17 T=0.83
HapMap Global Study-wide 1892 C=0.1808 T=0.8192
HapMap American Sub 770 C=0.130 T=0.870
HapMap African Sub 692 C=0.292 T=0.708
HapMap Asian Sub 254 C=0.094 T=0.906
HapMap Europe Sub 176 C=0.091 T=0.909
Korean Genome Project KOREAN Study-wide 1832 C=0.0862 T=0.9138
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 C=0.082 T=0.918
Northern Sweden ACPOP Study-wide 600 C=0.113 T=0.887
SGDP_PRJ Global Study-wide 538 C=0.095 T=0.905
Qatari Global Study-wide 216 C=0.171 T=0.829
A Vietnamese Genetic Variation Database Global Study-wide 214 C=0.098 T=0.902
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 56 C=0.04 T=0.96
Siberian Global Study-wide 56 C=0.04 T=0.96
The Danish reference pan genome Danish Study-wide 40 C=0.10 T=0.90
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 5 NC_000005.10:g.110742779C>A
GRCh38.p14 chr 5 NC_000005.10:g.110742779C>G
GRCh38.p14 chr 5 NC_000005.10:g.110742779C>T
GRCh37.p13 chr 5 NC_000005.9:g.110078480C>A
GRCh37.p13 chr 5 NC_000005.9:g.110078480C>G
GRCh37.p13 chr 5 NC_000005.9:g.110078480C>T
SLC25A46 RefSeqGene (LRG_1091) NG_051334.1:g.9644C>A
SLC25A46 RefSeqGene (LRG_1091) NG_051334.1:g.9644C>G
SLC25A46 RefSeqGene (LRG_1091) NG_051334.1:g.9644C>T
Gene: SLC25A46, solute carrier family 25 member 46 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
SLC25A46 transcript variant 2 NM_001303249.3:c.326+690C…

NM_001303249.3:c.326+690C>A

N/A Intron Variant
SLC25A46 transcript variant 3 NM_001303250.3:c.53+690C>A N/A Intron Variant
SLC25A46 transcript variant 1 NM_138773.4:c.326+690C>A N/A Intron Variant
SLC25A46 transcript variant 4 NR_138151.2:n. 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 C= A G T
GRCh38.p14 chr 5 NC_000005.10:g.110742779= NC_000005.10:g.110742779C>A NC_000005.10:g.110742779C>G NC_000005.10:g.110742779C>T
GRCh37.p13 chr 5 NC_000005.9:g.110078480= NC_000005.9:g.110078480C>A NC_000005.9:g.110078480C>G NC_000005.9:g.110078480C>T
SLC25A46 RefSeqGene (LRG_1091) NG_051334.1:g.9644= NG_051334.1:g.9644C>A NG_051334.1:g.9644C>G NG_051334.1:g.9644C>T
SLC25A46 transcript variant 2 NM_001303249.3:c.326+690= NM_001303249.3:c.326+690C>A NM_001303249.3:c.326+690C>G NM_001303249.3:c.326+690C>T
SLC25A46 transcript variant 3 NM_001303250.3:c.53+690= NM_001303250.3:c.53+690C>A NM_001303250.3:c.53+690C>G NM_001303250.3:c.53+690C>T
SLC25A46 transcript NM_138773.1:c.326+690= NM_138773.1:c.326+690C>A NM_138773.1:c.326+690C>G NM_138773.1:c.326+690C>T
SLC25A46 transcript variant 1 NM_138773.4:c.326+690= NM_138773.4:c.326+690C>A NM_138773.4:c.326+690C>G NM_138773.4:c.326+690C>T
SLC25A46 transcript variant X1 XM_005272126.1:c.326+690= XM_005272126.1:c.326+690C>A XM_005272126.1:c.326+690C>G XM_005272126.1:c.326+690C>T
SLC25A46 transcript variant X2 XM_005272127.1:c.53+690= XM_005272127.1:c.53+690C>A XM_005272127.1:c.53+690C>G XM_005272127.1:c.53+690C>T
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#.

121 SubSNP, 22 Frequency submissions
No Submitter Submission ID Date (Build)
1 KWOK ss314166 Jul 12, 2000 (79)
2 KWOK ss314836 Jul 12, 2000 (85)
3 SC_JCM ss477222 Jul 16, 2000 (80)
4 KWOK ss1116115 Oct 04, 2000 (86)
5 KWOK ss1117168 Oct 04, 2000 (86)
6 TSC-CSHL ss1317379 Oct 10, 2002 (110)
7 KWOK ss2033884 Oct 18, 2000 (87)
8 KWOK ss2034296 Oct 18, 2000 (87)
9 SC_JCM ss5923358 Feb 20, 2003 (111)
10 WI_SSAHASNP ss14642857 Dec 05, 2003 (119)
11 SSAHASNP ss22320777 Apr 05, 2004 (121)
12 PERLEGEN ss23316105 Sep 20, 2004 (123)
13 ABI ss44598045 Mar 14, 2006 (126)
14 ILLUMINA ss67254844 Nov 30, 2006 (127)
15 ILLUMINA ss67653020 Nov 30, 2006 (127)
16 ILLUMINA ss68205191 Dec 12, 2006 (127)
17 ILLUMINA ss70733194 May 25, 2008 (130)
18 ILLUMINA ss71302944 May 17, 2007 (127)
19 ILLUMINA ss74954652 Dec 07, 2007 (129)
20 KRIBB_YJKIM ss83400228 Dec 15, 2007 (130)
21 BCMHGSC_JDW ss93205656 Mar 24, 2008 (129)
22 HUMANGENOME_JCVI ss98638431 Feb 05, 2009 (130)
23 BGI ss105943677 Feb 05, 2009 (130)
24 1000GENOMES ss109307866 Jan 23, 2009 (130)
25 1000GENOMES ss112350126 Jan 25, 2009 (130)
26 ILLUMINA-UK ss116756015 Feb 14, 2009 (130)
27 ENSEMBL ss143226518 Dec 01, 2009 (131)
28 ENSEMBL ss143350717 Dec 01, 2009 (131)
29 ILLUMINA ss153912927 Dec 01, 2009 (131)
30 GMI ss155874568 Dec 01, 2009 (131)
31 ILLUMINA ss159390729 Dec 01, 2009 (131)
32 COMPLETE_GENOMICS ss162538953 Jul 04, 2010 (132)
33 COMPLETE_GENOMICS ss165688588 Jul 04, 2010 (132)
34 ILLUMINA ss173349054 Jul 04, 2010 (132)
35 BUSHMAN ss200672279 Jul 04, 2010 (132)
36 BCM-HGSC-SUB ss206741723 Jul 04, 2010 (132)
37 1000GENOMES ss221876681 Jul 14, 2010 (132)
38 1000GENOMES ss233087072 Jul 14, 2010 (132)
39 1000GENOMES ss240224424 Jul 15, 2010 (132)
40 GMI ss278425561 May 04, 2012 (137)
41 GMI ss285238331 Apr 25, 2013 (138)
42 PJP ss293432095 May 09, 2011 (134)
43 ILLUMINA ss480571934 May 04, 2012 (137)
44 ILLUMINA ss480586389 May 04, 2012 (137)
45 ILLUMINA ss485081513 May 04, 2012 (137)
46 ILLUMINA ss537091881 Sep 08, 2015 (146)
47 SSMP ss652504211 Apr 25, 2013 (138)
48 ILLUMINA ss778869494 Sep 08, 2015 (146)
49 ILLUMINA ss782987059 Sep 08, 2015 (146)
50 ILLUMINA ss783947943 Sep 08, 2015 (146)
51 ILLUMINA ss832243758 Sep 08, 2015 (146)
52 ILLUMINA ss832902478 Jul 13, 2019 (153)
53 ILLUMINA ss834330375 Sep 08, 2015 (146)
54 EVA-GONL ss981955461 Aug 21, 2014 (142)
55 JMKIDD_LAB ss1072918647 Aug 21, 2014 (142)
56 DDI ss1430456152 Apr 01, 2015 (144)
57 EVA_GENOME_DK ss1581285226 Apr 01, 2015 (144)
58 EVA_DECODE ss1591477243 Apr 01, 2015 (144)
59 EVA_UK10K_ALSPAC ss1613671255 Apr 01, 2015 (144)
60 EVA_UK10K_TWINSUK ss1656665288 Apr 01, 2015 (144)
61 EVA_SVP ss1712789162 Apr 01, 2015 (144)
62 ILLUMINA ss1752541819 Sep 08, 2015 (146)
63 HAMMER_LAB ss1804011440 Sep 08, 2015 (146)
64 WEILL_CORNELL_DGM ss1925209317 Feb 12, 2016 (147)
65 GENOMED ss1970174652 Jul 19, 2016 (147)
66 JJLAB ss2023211241 Sep 14, 2016 (149)
67 USC_VALOUEV ss2151367563 Dec 20, 2016 (150)
68 HUMAN_LONGEVITY ss2276816569 Dec 20, 2016 (150)
69 SYSTEMSBIOZJU ss2626097028 Nov 08, 2017 (151)
70 ILLUMINA ss2634321289 Nov 08, 2017 (151)
71 GRF ss2706925413 Nov 08, 2017 (151)
72 GNOMAD ss2828966831 Nov 08, 2017 (151)
73 SWEGEN ss2997539797 Nov 08, 2017 (151)
74 BIOINF_KMB_FNS_UNIBA ss3025388592 Nov 08, 2017 (151)
75 CSHL ss3346555673 Nov 08, 2017 (151)
76 ILLUMINA ss3629308957 Oct 12, 2018 (152)
77 ILLUMINA ss3632246252 Oct 12, 2018 (152)
78 ILLUMINA ss3633385142 Oct 12, 2018 (152)
79 ILLUMINA ss3634106124 Oct 12, 2018 (152)
80 ILLUMINA ss3635015816 Oct 12, 2018 (152)
81 ILLUMINA ss3635787952 Oct 12, 2018 (152)
82 ILLUMINA ss3637540588 Oct 12, 2018 (152)
83 ILLUMINA ss3638572473 Oct 12, 2018 (152)
84 ILLUMINA ss3639288822 Oct 12, 2018 (152)
85 ILLUMINA ss3639941512 Oct 12, 2018 (152)
86 ILLUMINA ss3640723110 Oct 12, 2018 (152)
87 ILLUMINA ss3643517104 Oct 12, 2018 (152)
88 ILLUMINA ss3643986923 Oct 12, 2018 (152)
89 URBANLAB ss3648138105 Oct 12, 2018 (152)
90 EGCUT_WGS ss3665437948 Jul 13, 2019 (153)
91 EVA_DECODE ss3715398769 Jul 13, 2019 (153)
92 ACPOP ss3732679912 Jul 13, 2019 (153)
93 ILLUMINA ss3745316036 Jul 13, 2019 (153)
94 EVA ss3763870136 Jul 13, 2019 (153)
95 ILLUMINA ss3772810084 Jul 13, 2019 (153)
96 PACBIO ss3785209306 Jul 13, 2019 (153)
97 PACBIO ss3790599416 Jul 13, 2019 (153)
98 PACBIO ss3795476192 Jul 13, 2019 (153)
99 KHV_HUMAN_GENOMES ss3807042426 Jul 13, 2019 (153)
100 EVA ss3829426026 Apr 26, 2020 (154)
101 EVA ss3838188816 Apr 26, 2020 (154)
102 EVA ss3843630731 Apr 26, 2020 (154)
103 HGDP ss3847801984 Apr 26, 2020 (154)
104 SGDP_PRJ ss3862646319 Apr 26, 2020 (154)
105 KRGDB ss3909258858 Apr 26, 2020 (154)
106 KOGIC ss3957366645 Apr 26, 2020 (154)
107 EVA ss3985161150 Apr 26, 2021 (155)
108 TOPMED ss4673166184 Apr 26, 2021 (155)
109 TOMMO_GENOMICS ss5173442680 Apr 26, 2021 (155)
110 1000G_HIGH_COVERAGE ss5265288566 Oct 17, 2022 (156)
111 EVA ss5315075479 Oct 17, 2022 (156)
112 EVA ss5359955094 Oct 17, 2022 (156)
113 HUGCELL_USP ss5463316070 Oct 17, 2022 (156)
114 1000G_HIGH_COVERAGE ss5549646617 Oct 17, 2022 (156)
115 SANFORD_IMAGENETICS ss5638561749 Oct 17, 2022 (156)
116 TOMMO_GENOMICS ss5710321936 Oct 17, 2022 (156)
117 YY_MCH ss5806635435 Oct 17, 2022 (156)
118 EVA ss5835429001 Oct 17, 2022 (156)
119 EVA ss5854956080 Oct 17, 2022 (156)
120 EVA ss5895679650 Oct 17, 2022 (156)
121 EVA ss5967010933 Oct 17, 2022 (156)
122 1000Genomes_30x NC_000005.10 - 110742779 Oct 17, 2022 (156)
123 The Avon Longitudinal Study of Parents and Children NC_000005.9 - 110078480 Oct 12, 2018 (152)
124 Genetic variation in the Estonian population NC_000005.9 - 110078480 Oct 12, 2018 (152)
125 The Danish reference pan genome NC_000005.9 - 110078480 Apr 26, 2020 (154)
126 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 199765889 (NC_000005.10:110742778:C:G 1/139988)
Row 199765890 (NC_000005.10:110742778:C:T 118475/139948)

- Apr 26, 2021 (155)
127 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 199765889 (NC_000005.10:110742778:C:G 1/139988)
Row 199765890 (NC_000005.10:110742778:C:T 118475/139948)

- Apr 26, 2021 (155)
128 Genome of the Netherlands Release 5 NC_000005.9 - 110078480 Apr 26, 2020 (154)
129 HGDP-CEPH-db Supplement 1 NC_000005.8 - 110106379 Apr 26, 2020 (154)
130 HapMap NC_000005.10 - 110742779 Apr 26, 2020 (154)
131 KOREAN population from KRGDB NC_000005.9 - 110078480 Apr 26, 2020 (154)
132 Korean Genome Project NC_000005.10 - 110742779 Apr 26, 2020 (154)
133 Northern Sweden NC_000005.9 - 110078480 Jul 13, 2019 (153)
134 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000005.9 - 110078480 Apr 26, 2021 (155)
135 Qatari NC_000005.9 - 110078480 Apr 26, 2020 (154)
136 SGDP_PRJ NC_000005.9 - 110078480 Apr 26, 2020 (154)
137 Siberian NC_000005.9 - 110078480 Apr 26, 2020 (154)
138 8.3KJPN NC_000005.9 - 110078480 Apr 26, 2021 (155)
139 14KJPN NC_000005.10 - 110742779 Oct 17, 2022 (156)
140 TopMed NC_000005.10 - 110742779 Apr 26, 2021 (155)
141 UK 10K study - Twins NC_000005.9 - 110078480 Oct 12, 2018 (152)
142 A Vietnamese Genetic Variation Database NC_000005.9 - 110078480 Jul 13, 2019 (153)
143 ALFA NC_000005.10 - 110742779 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)
rs244925 Sep 19, 2000 (85)
rs3893701 Dec 16, 2002 (110)
rs59673669 May 25, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
16436252, ss3909258858 NC_000005.9:110078479:C:A NC_000005.10:110742778:C:A (self)
16436252, ss3909258858 NC_000005.9:110078479:C:G NC_000005.10:110742778:C:G (self)
10953882465 NC_000005.10:110742778:C:G NC_000005.10:110742778:C:G (self)
479876, ss93205656, ss109307866, ss112350126, ss116756015, ss162538953, ss165688588, ss200672279, ss206741723, ss278425561, ss285238331, ss293432095, ss480571934, ss1591477243, ss1712789162, ss3639288822, ss3639941512, ss3643517104, ss3643986923, ss3847801984 NC_000005.8:110106378:C:T NC_000005.10:110742778:C:T (self)
15700810, 11176196, 7450165, 6978210, 16436252, 5964777, 387077, 7251247, 14663299, 3883917, 31411987, 15700810, 3483714, ss221876681, ss233087072, ss240224424, ss480586389, ss485081513, ss537091881, ss652504211, ss778869494, ss782987059, ss783947943, ss832243758, ss832902478, ss834330375, ss981955461, ss1072918647, ss1430456152, ss1581285226, ss1613671255, ss1656665288, ss1752541819, ss1804011440, ss1925209317, ss1970174652, ss2023211241, ss2151367563, ss2626097028, ss2634321289, ss2706925413, ss2828966831, ss2997539797, ss3346555673, ss3629308957, ss3632246252, ss3633385142, ss3634106124, ss3635015816, ss3635787952, ss3637540588, ss3638572473, ss3640723110, ss3665437948, ss3732679912, ss3745316036, ss3763870136, ss3772810084, ss3785209306, ss3790599416, ss3795476192, ss3829426026, ss3838188816, ss3862646319, ss3909258858, ss3985161150, ss5173442680, ss5315075479, ss5359955094, ss5638561749, ss5835429001, ss5967010933 NC_000005.9:110078479:C:T NC_000005.10:110742778:C:T (self)
37172552, 2937788, 13744646, 44159040, 510543741, 10953882465, ss2276816569, ss3025388592, ss3648138105, ss3715398769, ss3807042426, ss3843630731, ss3957366645, ss4673166184, ss5265288566, ss5463316070, ss5549646617, ss5710321936, ss5806635435, ss5854956080, ss5895679650 NC_000005.10:110742778:C:T NC_000005.10:110742778:C:T (self)
ss14642857, ss22320777 NT_034772.5:12493492:C:T NC_000005.10:110742778:C:T (self)
ss314166, ss314836, ss477222, ss1116115, ss1117168, ss1317379, ss2033884, ss2034296, ss5923358, ss23316105, ss44598045, ss67254844, ss67653020, ss68205191, ss70733194, ss71302944, ss74954652, ss83400228, ss98638431, ss105943677, ss143226518, ss143350717, ss153912927, ss155874568, ss159390729, ss173349054 NT_034772.6:18392351:C:T NC_000005.10:110742778:C:T (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 rs244411

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