Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

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.

rs897762

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr19:35116093 (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 / G>C
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.037244 (9858/264690, TOPMED)
G=0.034184 (4792/140184, GnomAD)
G=0.05265 (4143/78690, PAGE_STUDY) (+ 17 more)
G=0.00418 (118/28258, 14KJPN)
G=0.03158 (668/21152, ALFA)
G=0.00430 (72/16760, 8.3KJPN)
G=0.0372 (238/6404, 1000G_30x)
G=0.0357 (179/5008, 1000G)
G=0.0036 (14/3854, ALSPAC)
G=0.0003 (1/3708, TWINSUK)
G=0.0119 (35/2930, KOREAN)
G=0.0071 (13/1832, Korea1K)
G=0.004 (4/998, GoNL)
G=0.000 (0/600, NorthernSweden)
G=0.027 (15/550, SGDP_PRJ)
G=0.038 (12/318, HapMap)
G=0.042 (9/216, Qatari)
G=0.033 (7/212, Vietnamese)
G=0.00 (0/56, Siberian)
G=0.00 (0/40, GENOME_DK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
FXYD3 : 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 21152 G=0.03158 A=0.96842, C=0.00000
European Sub 13708 G=0.00117 A=0.99883, C=0.00000
African Sub 5490 G=0.1102 A=0.8898, C=0.0000
African Others Sub 174 G=0.063 A=0.937, C=0.000
African American Sub 5316 G=0.1117 A=0.8883, C=0.0000
Asian Sub 146 G=0.021 A=0.979, C=0.000
East Asian Sub 120 G=0.017 A=0.983, C=0.000
Other Asian Sub 26 G=0.04 A=0.96, C=0.00
Latin American 1 Sub 146 G=0.014 A=0.986, C=0.000
Latin American 2 Sub 610 G=0.011 A=0.989, C=0.000
South Asian Sub 104 G=0.038 A=0.962, C=0.000
Other Sub 948 G=0.033 A=0.967, C=0.000


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=0.037244 A=0.962756
gnomAD - Genomes Global Study-wide 140184 G=0.034184 A=0.965816
gnomAD - Genomes European Sub 75946 G=0.00137 A=0.99863
gnomAD - Genomes African Sub 41970 G=0.10405 A=0.89595
gnomAD - Genomes American Sub 13662 G=0.01603 A=0.98397
gnomAD - Genomes Ashkenazi Jewish Sub 3324 G=0.0102 A=0.9898
gnomAD - Genomes East Asian Sub 3132 G=0.0073 A=0.9927
gnomAD - Genomes Other Sub 2150 G=0.0209 A=0.9791
The PAGE Study Global Study-wide 78690 G=0.05265 A=0.94735
The PAGE Study AfricanAmerican Sub 32508 G=0.10154 A=0.89846
The PAGE Study Mexican Sub 10810 G=0.00601 A=0.99399
The PAGE Study Asian Sub 8318 G=0.0103 A=0.9897
The PAGE Study PuertoRican Sub 7918 G=0.0354 A=0.9646
The PAGE Study NativeHawaiian Sub 4532 G=0.0086 A=0.9914
The PAGE Study Cuban Sub 4230 G=0.0139 A=0.9861
The PAGE Study Dominican Sub 3826 G=0.0486 A=0.9514
The PAGE Study CentralAmerican Sub 2450 G=0.0171 A=0.9829
The PAGE Study SouthAmerican Sub 1982 G=0.0141 A=0.9859
The PAGE Study NativeAmerican Sub 1260 G=0.0238 A=0.9762
The PAGE Study SouthAsian Sub 856 G=0.032 A=0.968
14KJPN JAPANESE Study-wide 28258 G=0.00418 A=0.99582
Allele Frequency Aggregator Total Global 21152 G=0.03158 A=0.96842, C=0.00000
Allele Frequency Aggregator European Sub 13708 G=0.00117 A=0.99883, C=0.00000
Allele Frequency Aggregator African Sub 5490 G=0.1102 A=0.8898, C=0.0000
Allele Frequency Aggregator Other Sub 948 G=0.033 A=0.967, C=0.000
Allele Frequency Aggregator Latin American 2 Sub 610 G=0.011 A=0.989, C=0.000
Allele Frequency Aggregator Latin American 1 Sub 146 G=0.014 A=0.986, C=0.000
Allele Frequency Aggregator Asian Sub 146 G=0.021 A=0.979, C=0.000
Allele Frequency Aggregator South Asian Sub 104 G=0.038 A=0.962, C=0.000
8.3KJPN JAPANESE Study-wide 16760 G=0.00430 A=0.99570
1000Genomes_30x Global Study-wide 6404 G=0.0372 A=0.9628
1000Genomes_30x African Sub 1786 G=0.0946 A=0.9054
1000Genomes_30x Europe Sub 1266 G=0.0016 A=0.9984
1000Genomes_30x South Asian Sub 1202 G=0.0341 A=0.9659
1000Genomes_30x East Asian Sub 1170 G=0.0111 A=0.9889
1000Genomes_30x American Sub 980 G=0.013 A=0.987
1000Genomes Global Study-wide 5008 G=0.0357 A=0.9643
1000Genomes African Sub 1322 G=0.0915 A=0.9085
1000Genomes East Asian Sub 1008 G=0.0119 A=0.9881
1000Genomes Europe Sub 1006 G=0.0010 A=0.9990
1000Genomes South Asian Sub 978 G=0.037 A=0.963
1000Genomes American Sub 694 G=0.013 A=0.987
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.0036 A=0.9964
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.0003 A=0.9997
KOREAN population from KRGDB KOREAN Study-wide 2930 G=0.0119 A=0.9881, C=0.0000
Korean Genome Project KOREAN Study-wide 1832 G=0.0071 A=0.9929
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.004 A=0.996
Northern Sweden ACPOP Study-wide 600 G=0.000 A=1.000
SGDP_PRJ Global Study-wide 550 G=0.027 A=0.973
HapMap Global Study-wide 318 G=0.038 A=0.962
HapMap American Sub 116 G=0.000 A=1.000
HapMap African Sub 114 G=0.105 A=0.895
HapMap Asian Sub 88 G=0.00 A=1.00
Qatari Global Study-wide 216 G=0.042 A=0.958
A Vietnamese Genetic Variation Database Global Study-wide 212 G=0.033 A=0.967
Siberian Global Study-wide 56 G=0.00 A=1.00
The Danish reference pan genome Danish Study-wide 40 G=0.00 A=1.00
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 19 NC_000019.10:g.35116093G>A
GRCh38.p14 chr 19 NC_000019.10:g.35116093G>C
GRCh37.p13 chr 19 NC_000019.9:g.35606997G>A
GRCh37.p13 chr 19 NC_000019.9:g.35606997G>C
Gene: FXYD3, FXYD domain containing ion transport regulator 3 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
FXYD3 transcript variant 3 NM_001136007.2:c.-146+134…

NM_001136007.2:c.-146+134G>A

N/A Intron Variant
FXYD3 transcript variant 4 NM_001136008.2:c.-111+134…

NM_001136008.2:c.-111+134G>A

N/A Intron Variant
FXYD3 transcript variant 5 NM_001136009.2:c.-195+134…

NM_001136009.2:c.-195+134G>A

N/A Intron Variant
FXYD3 transcript variant 6 NM_001136010.2:c.-111+134…

NM_001136010.2:c.-111+134G>A

N/A Intron Variant
FXYD3 transcript variant 7 NM_001136011.2:c.-195+134…

NM_001136011.2:c.-195+134G>A

N/A Intron Variant
FXYD3 transcript variant 8 NM_001136012.2:c.-111+134…

NM_001136012.2:c.-111+134G>A

N/A Intron Variant
FXYD3 transcript variant 9 NM_001387349.1:c.-195+53G…

NM_001387349.1:c.-195+53G>A

N/A Intron Variant
FXYD3 transcript variant 10 NM_001387350.1:c.-111+53G…

NM_001387350.1:c.-111+53G>A

N/A Intron Variant
FXYD3 transcript variant 14 NM_001387355.1:c.-146+53G…

NM_001387355.1:c.-146+53G>A

N/A Intron Variant
FXYD3 transcript variant 1 NM_005971.4:c.-111+134G>A N/A Intron Variant
FXYD3 transcript variant 2 NM_021910.3:c.-195+134G>A N/A Intron Variant
FXYD3 transcript variant 11 NM_001387352.1:c. N/A Genic Upstream Transcript Variant
FXYD3 transcript variant 12 NM_001387353.1:c. N/A Genic Upstream Transcript Variant
FXYD3 transcript variant 13 NM_001387354.1:c. N/A Genic Upstream Transcript 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 C
GRCh38.p14 chr 19 NC_000019.10:g.35116093= NC_000019.10:g.35116093G>A NC_000019.10:g.35116093G>C
GRCh37.p13 chr 19 NC_000019.9:g.35606997= NC_000019.9:g.35606997G>A NC_000019.9:g.35606997G>C
FXYD3 transcript variant 3 NM_001136007.1:c.-146+134= NM_001136007.1:c.-146+134G>A NM_001136007.1:c.-146+134G>C
FXYD3 transcript variant 3 NM_001136007.2:c.-146+134= NM_001136007.2:c.-146+134G>A NM_001136007.2:c.-146+134G>C
FXYD3 transcript variant 4 NM_001136008.1:c.-111+134= NM_001136008.1:c.-111+134G>A NM_001136008.1:c.-111+134G>C
FXYD3 transcript variant 4 NM_001136008.2:c.-111+134= NM_001136008.2:c.-111+134G>A NM_001136008.2:c.-111+134G>C
FXYD3 transcript variant 5 NM_001136009.1:c.-195+134= NM_001136009.1:c.-195+134G>A NM_001136009.1:c.-195+134G>C
FXYD3 transcript variant 5 NM_001136009.2:c.-195+134= NM_001136009.2:c.-195+134G>A NM_001136009.2:c.-195+134G>C
FXYD3 transcript variant 6 NM_001136010.1:c.-111+134= NM_001136010.1:c.-111+134G>A NM_001136010.1:c.-111+134G>C
FXYD3 transcript variant 6 NM_001136010.2:c.-111+134= NM_001136010.2:c.-111+134G>A NM_001136010.2:c.-111+134G>C
FXYD3 transcript variant 7 NM_001136011.1:c.-195+134= NM_001136011.1:c.-195+134G>A NM_001136011.1:c.-195+134G>C
FXYD3 transcript variant 7 NM_001136011.2:c.-195+134= NM_001136011.2:c.-195+134G>A NM_001136011.2:c.-195+134G>C
FXYD3 transcript variant 8 NM_001136012.1:c.-111+134= NM_001136012.1:c.-111+134G>A NM_001136012.1:c.-111+134G>C
FXYD3 transcript variant 8 NM_001136012.2:c.-111+134= NM_001136012.2:c.-111+134G>A NM_001136012.2:c.-111+134G>C
FXYD3 transcript variant 9 NM_001387349.1:c.-195+53= NM_001387349.1:c.-195+53G>A NM_001387349.1:c.-195+53G>C
FXYD3 transcript variant 10 NM_001387350.1:c.-111+53= NM_001387350.1:c.-111+53G>A NM_001387350.1:c.-111+53G>C
FXYD3 transcript variant 14 NM_001387355.1:c.-146+53= NM_001387355.1:c.-146+53G>A NM_001387355.1:c.-146+53G>C
FXYD3 transcript variant 1 NM_005971.3:c.-111+134= NM_005971.3:c.-111+134G>A NM_005971.3:c.-111+134G>C
FXYD3 transcript variant 1 NM_005971.4:c.-111+134= NM_005971.4:c.-111+134G>A NM_005971.4:c.-111+134G>C
FXYD3 transcript variant 2 NM_021910.2:c.-195+134= NM_021910.2:c.-195+134G>A NM_021910.2:c.-195+134G>C
FXYD3 transcript variant 2 NM_021910.3:c.-195+134= NM_021910.3:c.-195+134G>A NM_021910.3:c.-195+134G>C
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#.

83 SubSNP, 20 Frequency submissions
No Submitter Submission ID Date (Build)
1 TSC-CSHL ss1328626 Oct 05, 2000 (86)
2 SC_JCM ss2500161 Nov 08, 2000 (89)
3 SC_JCM ss5692199 Feb 20, 2003 (111)
4 BCM_SSAHASNP ss14693333 Dec 05, 2003 (119)
5 CSHL-HAPMAP ss16786924 Feb 27, 2004 (120)
6 CSHL-HAPMAP ss19395417 Feb 27, 2004 (120)
7 SSAHASNP ss21514760 Apr 05, 2004 (123)
8 HGSV ss77291122 Dec 07, 2007 (129)
9 HGSV ss78784824 Dec 07, 2007 (129)
10 BCMHGSC_JDW ss90962419 Mar 24, 2008 (129)
11 HUMANGENOME_JCVI ss96265944 Feb 06, 2009 (130)
12 BGI ss106054105 Feb 06, 2009 (130)
13 1000GENOMES ss111338454 Jan 25, 2009 (130)
14 1000GENOMES ss115089776 Jan 25, 2009 (130)
15 ILLUMINA-UK ss117695506 Feb 14, 2009 (130)
16 ENSEMBL ss136273445 Dec 01, 2009 (131)
17 ENSEMBL ss137659296 Dec 01, 2009 (131)
18 GMI ss155862057 Dec 01, 2009 (131)
19 COMPLETE_GENOMICS ss168148972 Jul 04, 2010 (132)
20 COMPLETE_GENOMICS ss169642029 Jul 04, 2010 (132)
21 COMPLETE_GENOMICS ss171732857 Jul 04, 2010 (132)
22 BUSHMAN ss203743874 Jul 04, 2010 (132)
23 1000GENOMES ss228125960 Jul 14, 2010 (132)
24 1000GENOMES ss237666886 Jul 15, 2010 (132)
25 1000GENOMES ss243874448 Jul 15, 2010 (132)
26 BL ss255651791 May 09, 2011 (134)
27 GMI ss283196990 May 04, 2012 (137)
28 GMI ss287378606 Apr 25, 2013 (138)
29 PJP ss292244708 May 09, 2011 (134)
30 TISHKOFF ss565963192 Apr 25, 2013 (138)
31 SSMP ss661824815 Apr 25, 2013 (138)
32 EVA-GONL ss994266415 Aug 21, 2014 (142)
33 JMKIDD_LAB ss1081881810 Aug 21, 2014 (142)
34 1000GENOMES ss1363036369 Aug 21, 2014 (142)
35 DDI ss1428394622 Apr 01, 2015 (144)
36 EVA_GENOME_DK ss1578627579 Apr 01, 2015 (144)
37 EVA_UK10K_ALSPAC ss1637905355 Apr 01, 2015 (144)
38 EVA_UK10K_TWINSUK ss1680899388 Apr 01, 2015 (144)
39 HAMMER_LAB ss1809292576 Sep 08, 2015 (146)
40 WEILL_CORNELL_DGM ss1937760093 Feb 12, 2016 (147)
41 ILLUMINA ss1959858634 Feb 12, 2016 (147)
42 GENOMED ss1968637865 Jul 19, 2016 (147)
43 JJLAB ss2029657845 Sep 14, 2016 (149)
44 USC_VALOUEV ss2158196288 Dec 20, 2016 (150)
45 HUMAN_LONGEVITY ss2225510319 Dec 20, 2016 (150)
46 SYSTEMSBIOZJU ss2629326158 Nov 08, 2017 (151)
47 GRF ss2702804650 Nov 08, 2017 (151)
48 GNOMAD ss2962478740 Nov 08, 2017 (151)
49 SWEGEN ss3017413697 Nov 08, 2017 (151)
50 ILLUMINA ss3021900378 Nov 08, 2017 (151)
51 CSHL ss3352287941 Nov 08, 2017 (151)
52 BIOINF_KMB_FNS_UNIBA ss3645519241 Oct 12, 2018 (152)
53 URBANLAB ss3650910588 Oct 12, 2018 (152)
54 ILLUMINA ss3652326220 Oct 12, 2018 (152)
55 EVA_DECODE ss3702701491 Jul 13, 2019 (153)
56 ILLUMINA ss3725724373 Jul 13, 2019 (153)
57 ACPOP ss3743009888 Jul 13, 2019 (153)
58 EVA ss3756025150 Jul 13, 2019 (153)
59 PAGE_CC ss3772009829 Jul 13, 2019 (153)
60 PACBIO ss3788520608 Jul 13, 2019 (153)
61 PACBIO ss3793432992 Jul 13, 2019 (153)
62 PACBIO ss3798319741 Jul 13, 2019 (153)
63 KHV_HUMAN_GENOMES ss3821273142 Jul 13, 2019 (153)
64 EVA ss3835445815 Apr 27, 2020 (154)
65 EVA ss3841345328 Apr 27, 2020 (154)
66 EVA ss3846851143 Apr 27, 2020 (154)
67 SGDP_PRJ ss3888146673 Apr 27, 2020 (154)
68 KRGDB ss3938239074 Apr 27, 2020 (154)
69 KOGIC ss3981268501 Apr 27, 2020 (154)
70 TOPMED ss5073716181 Apr 27, 2021 (155)
71 TOMMO_GENOMICS ss5227589864 Apr 27, 2021 (155)
72 1000G_HIGH_COVERAGE ss5307128022 Oct 16, 2022 (156)
73 EVA ss5434635131 Oct 16, 2022 (156)
74 HUGCELL_USP ss5499669435 Oct 16, 2022 (156)
75 1000G_HIGH_COVERAGE ss5612806011 Oct 16, 2022 (156)
76 SANFORD_IMAGENETICS ss5662326068 Oct 16, 2022 (156)
77 TOMMO_GENOMICS ss5786167430 Oct 16, 2022 (156)
78 YY_MCH ss5817570343 Oct 16, 2022 (156)
79 EVA ss5840504347 Oct 16, 2022 (156)
80 EVA ss5852276241 Oct 16, 2022 (156)
81 EVA ss5927976647 Oct 16, 2022 (156)
82 EVA ss5953742029 Oct 16, 2022 (156)
83 EVA ss5981049368 Oct 16, 2022 (156)
84 1000Genomes NC_000019.9 - 35606997 Oct 12, 2018 (152)
85 1000Genomes_30x NC_000019.10 - 35116093 Oct 16, 2022 (156)
86 The Avon Longitudinal Study of Parents and Children NC_000019.9 - 35606997 Oct 12, 2018 (152)
87 The Danish reference pan genome NC_000019.9 - 35606997 Apr 27, 2020 (154)
88 gnomAD - Genomes NC_000019.10 - 35116093 Apr 27, 2021 (155)
89 Genome of the Netherlands Release 5 NC_000019.9 - 35606997 Apr 27, 2020 (154)
90 HapMap NC_000019.10 - 35116093 Apr 27, 2020 (154)
91 KOREAN population from KRGDB NC_000019.9 - 35606997 Apr 27, 2020 (154)
92 Korean Genome Project NC_000019.10 - 35116093 Apr 27, 2020 (154)
93 Northern Sweden NC_000019.9 - 35606997 Jul 13, 2019 (153)
94 The PAGE Study NC_000019.10 - 35116093 Jul 13, 2019 (153)
95 Qatari NC_000019.9 - 35606997 Apr 27, 2020 (154)
96 SGDP_PRJ NC_000019.9 - 35606997 Apr 27, 2020 (154)
97 Siberian NC_000019.9 - 35606997 Apr 27, 2020 (154)
98 8.3KJPN NC_000019.9 - 35606997 Apr 27, 2021 (155)
99 14KJPN NC_000019.10 - 35116093 Oct 16, 2022 (156)
100 TopMed NC_000019.10 - 35116093 Apr 27, 2021 (155)
101 UK 10K study - Twins NC_000019.9 - 35606997 Oct 12, 2018 (152)
102 A Vietnamese Genetic Variation Database NC_000019.9 - 35606997 Jul 13, 2019 (153)
103 ALFA NC_000019.10 - 35116093 Apr 27, 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)
rs12973715 Sep 24, 2004 (123)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss77291122, ss78784824, ss90962419, ss111338454, ss115089776, ss117695506, ss168148972, ss169642029, ss171732857, ss203743874, ss255651791, ss283196990, ss287378606, ss292244708 NC_000019.8:40298836:G:A NC_000019.10:35116092:G:A (self)
76438754, 42339616, 4810610, 18862232, 45416468, 16294753, 19802015, 40163653, 10712642, 85559171, 42339616, 9353103, ss228125960, ss237666886, ss243874448, ss565963192, ss661824815, ss994266415, ss1081881810, ss1363036369, ss1428394622, ss1578627579, ss1637905355, ss1680899388, ss1809292576, ss1937760093, ss1959858634, ss1968637865, ss2029657845, ss2158196288, ss2629326158, ss2702804650, ss2962478740, ss3017413697, ss3021900378, ss3352287941, ss3652326220, ss3743009888, ss3756025150, ss3788520608, ss3793432992, ss3798319741, ss3835445815, ss3841345328, ss3888146673, ss3938239074, ss5227589864, ss5434635131, ss5662326068, ss5840504347, ss5953742029, ss5981049368 NC_000019.9:35606996:G:A NC_000019.10:35116092:G:A (self)
100331946, 539084409, 1691522, 37646502, 1231298, 120004534, 289261845, 2217496749, ss2225510319, ss3645519241, ss3650910588, ss3702701491, ss3725724373, ss3772009829, ss3821273142, ss3846851143, ss3981268501, ss5073716181, ss5307128022, ss5499669435, ss5612806011, ss5786167430, ss5817570343, ss5852276241, ss5927976647 NC_000019.10:35116092:G:A NC_000019.10:35116092:G:A (self)
ss14693333, ss16786924, ss19395417, ss21514760 NT_011109.15:7875214:G:A NC_000019.10:35116092:G:A (self)
ss1328626, ss2500161, ss5692199, ss96265944, ss106054105, ss136273445, ss137659296, ss155862057 NT_011109.16:7875214:G:A NC_000019.10:35116092:G:A (self)
45416468, ss3938239074 NC_000019.9:35606996:G:C NC_000019.10:35116092:G:C (self)
2217496749 NC_000019.10:35116092:G:C NC_000019.10:35116092:G:C (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 rs897762

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