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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.

rs850610

Current Build 155

Released April 9, 2021

Organism
Homo sapiens
Position
chr1:116406090 (GRCh38.p13) 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 / G>T
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.463304 (122632/264690, TOPMED)
G=0.354393 (72562/204750, ALFA)
A=0.486268 (68024/139890, GnomAD) (+ 18 more)
A=0.33192 (5563/16760, 8.3KJPN)
A=0.4181 (2094/5008, 1000G)
G=0.3391 (1519/4480, Estonian)
G=0.3067 (1182/3854, ALSPAC)
G=0.3026 (1122/3708, TWINSUK)
A=0.2829 (829/2930, KOREAN)
A=0.4391 (915/2084, HGDP_Stanford)
A=0.3531 (668/1892, HapMap)
A=0.2587 (474/1832, Korea1K)
G=0.274 (273/998, GoNL)
G=0.362 (217/600, NorthernSweden)
G=0.354 (189/534, MGP)
G=0.303 (95/314, SGDP_PRJ)
G=0.491 (106/216, Qatari)
A=0.238 (50/210, Vietnamese)
A=0.45 (34/76, Ancient Sardinia)
G=0.19 (8/42, Siberian)
G=0.28 (11/40, GENOME_DK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
ATP1A1-AS1 : Non Coding Transcript Variant
ATP1A1 : Non Coding Transcript Variant
Publications
1 citation
Genomic View
See rs on genome
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.p13 chr 1 NC_000001.11:g.116406090G>A
GRCh38.p13 chr 1 NC_000001.11:g.116406090G>C
GRCh38.p13 chr 1 NC_000001.11:g.116406090G>T
GRCh37.p13 chr 1 NC_000001.10:g.116948712G>A
GRCh37.p13 chr 1 NC_000001.10:g.116948712G>C
GRCh37.p13 chr 1 NC_000001.10:g.116948712G>T
ATP1A1 RefSeqGene NG_047036.1:g.38906G>A
ATP1A1 RefSeqGene NG_047036.1:g.38906G>C
ATP1A1 RefSeqGene NG_047036.1:g.38906G>T
Gene: ATP1A1, ATPase Na+/K+ transporting subunit alpha 1 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
ATP1A1 transcript variant 1 NM_000701.8:c. N/A Genic Downstream Transcript Variant
ATP1A1 transcript variant 3 NM_001160233.2:c. N/A Genic Downstream Transcript Variant
ATP1A1 transcript variant 4 NM_001160234.2:c. N/A Genic Downstream Transcript Variant
ATP1A1 transcript variant X1 XM_017001360.1:c. N/A Genic Downstream Transcript Variant
ATP1A1 transcript variant X2 XM_017001361.1:c. N/A Genic Downstream Transcript Variant
ATP1A1 transcript variant X3 XR_002956654.1:n.6684G>A N/A Non Coding Transcript Variant
ATP1A1 transcript variant X3 XR_002956654.1:n.6684G>C N/A Non Coding Transcript Variant
ATP1A1 transcript variant X3 XR_002956654.1:n.6684G>T N/A Non Coding Transcript Variant
Gene: ATP1A1-AS1, ATP1A1 antisense RNA 1 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
ATP1A1-AS1 transcript variant 3 NR_024126.1:n.215C>T N/A Non Coding Transcript Variant
ATP1A1-AS1 transcript variant 3 NR_024126.1:n.215C>G N/A Non Coding Transcript Variant
ATP1A1-AS1 transcript variant 3 NR_024126.1:n.215C>A N/A Non Coding Transcript Variant
ATP1A1-AS1 transcript variant 5 NR_024124.2:n.176C>T N/A Non Coding Transcript Variant
ATP1A1-AS1 transcript variant 5 NR_024124.2:n.176C>G N/A Non Coding Transcript Variant
ATP1A1-AS1 transcript variant 5 NR_024124.2:n.176C>A N/A Non Coding Transcript Variant
ATP1A1-AS1 transcript variant 4 NR_024125.2:n.452C>T N/A Non Coding Transcript Variant
ATP1A1-AS1 transcript variant 4 NR_024125.2:n.452C>G N/A Non Coding Transcript Variant
ATP1A1-AS1 transcript variant 4 NR_024125.2:n.452C>A N/A Non Coding Transcript Variant
ATP1A1-AS1 transcript variant 2 NR_027645.1:n. N/A Intron Variant
ATP1A1-AS1 transcript variant 1 NR_027646.1: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

ALFA Allele Frequency (New)
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: 20201027095038
Population Group Sample Size Ref Allele Alt Allele
Total Global 204750 G=0.354393 A=0.645607
European Sub 177240 G=0.324030 A=0.675970
African Sub 7094 G=0.8510 A=0.1490
African Others Sub 264 G=0.932 A=0.068
African American Sub 6830 G=0.8479 A=0.1521
Asian Sub 702 G=0.712 A=0.288
East Asian Sub 556 G=0.700 A=0.300
Other Asian Sub 146 G=0.760 A=0.240
Latin American 1 Sub 842 G=0.514 A=0.486
Latin American 2 Sub 6904 G=0.5552 A=0.4448
South Asian Sub 5042 G=0.2713 A=0.7287
Other Sub 6926 G=0.4274 A=0.5726


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=0.536696 A=0.463304
gnomAD - Genomes Global Study-wide 139890 G=0.513732 A=0.486268
gnomAD - Genomes European Sub 75814 G=0.33076 A=0.66924
gnomAD - Genomes African Sub 41886 G=0.84797 A=0.15203
gnomAD - Genomes American Sub 13626 G=0.48385 A=0.51615
gnomAD - Genomes Ashkenazi Jewish Sub 3314 G=0.4309 A=0.5691
gnomAD - Genomes East Asian Sub 3108 G=0.7050 A=0.2950
gnomAD - Genomes Other Sub 2142 G=0.4949 A=0.5051
8.3KJPN JAPANESE Study-wide 16760 G=0.66808 A=0.33192
1000Genomes Global Study-wide 5008 G=0.5819 A=0.4181
1000Genomes African Sub 1322 G=0.9440 A=0.0560
1000Genomes East Asian Sub 1008 G=0.7331 A=0.2669
1000Genomes Europe Sub 1006 G=0.3370 A=0.6630
1000Genomes South Asian Sub 978 G=0.254 A=0.746
1000Genomes American Sub 694 G=0.490 A=0.510
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.3391 A=0.6609
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.3067 A=0.6933
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.3026 A=0.6974
KOREAN population from KRGDB KOREAN Study-wide 2930 G=0.7171 A=0.2829
HGDP-CEPH-db Supplement 1 Global Study-wide 2084 G=0.5609 A=0.4391
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 G=0.755 A=0.245
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 G=0.341 A=0.659
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 G=0.440 A=0.560
HGDP-CEPH-db Supplement 1 Europe Sub 320 G=0.306 A=0.694
HGDP-CEPH-db Supplement 1 Africa Sub 242 G=0.950 A=0.050
HGDP-CEPH-db Supplement 1 America Sub 216 G=0.685 A=0.315
HGDP-CEPH-db Supplement 1 Oceania Sub 72 G=0.60 A=0.40
HapMap Global Study-wide 1892 G=0.6469 A=0.3531
HapMap American Sub 770 G=0.481 A=0.519
HapMap African Sub 692 G=0.899 A=0.101
HapMap Asian Sub 254 G=0.677 A=0.323
HapMap Europe Sub 176 G=0.341 A=0.659
Korean Genome Project KOREAN Study-wide 1832 G=0.7413 A=0.2587
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.274 A=0.726
Northern Sweden ACPOP Study-wide 600 G=0.362 A=0.638
Medical Genome Project healthy controls from Spanish population Spanish controls Study-wide 534 G=0.354 A=0.646
SGDP_PRJ Global Study-wide 314 G=0.303 A=0.697
Qatari Global Study-wide 216 G=0.491 A=0.509
A Vietnamese Genetic Variation Database Global Study-wide 210 G=0.762 A=0.238
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 76 G=0.55 A=0.45
Siberian Global Study-wide 42 G=0.19 A=0.81
The Danish reference pan genome Danish Study-wide 40 G=0.28 A=0.72
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 T
GRCh38.p13 chr 1 NC_000001.11:g.116406090= NC_000001.11:g.116406090G>A NC_000001.11:g.116406090G>C NC_000001.11:g.116406090G>T
GRCh37.p13 chr 1 NC_000001.10:g.116948712= NC_000001.10:g.116948712G>A NC_000001.10:g.116948712G>C NC_000001.10:g.116948712G>T
ATP1A1 RefSeqGene NG_047036.1:g.38906= NG_047036.1:g.38906G>A NG_047036.1:g.38906G>C NG_047036.1:g.38906G>T
ATP1A1-AS1 transcript variant 4 NR_024125.2:n.452= NR_024125.2:n.452C>T NR_024125.2:n.452C>G NR_024125.2:n.452C>A
ATP1A1-AS1 transcript variant 5 NR_024124.2:n.176= NR_024124.2:n.176C>T NR_024124.2:n.176C>G NR_024124.2:n.176C>A
ATP1A1 transcript variant X3 XR_002956654.1:n.6684= XR_002956654.1:n.6684G>A XR_002956654.1:n.6684G>C XR_002956654.1:n.6684G>T
ATP1A1-AS1 transcript variant 3 NR_024126.1:n.215= NR_024126.1:n.215C>T NR_024126.1:n.215C>G NR_024126.1:n.215C>A
MGC16179 transcript NM_032766.1:c.68= NM_032766.1:c.68C>T NM_032766.1:c.68C>G NM_032766.1:c.68C>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#.

119 SubSNP, 21 Frequency submissions
No Submitter Submission ID Date (Build)
1 KWOK ss1221796 Oct 05, 2000 (86)
2 KWOK ss1647969 Oct 18, 2000 (87)
3 TSC-CSHL ss2733230 Jan 22, 2001 (92)
4 WI_SSAHASNP ss6683640 Feb 20, 2003 (111)
5 CGAP-GAI ss16253084 Feb 27, 2004 (120)
6 CSHL-HAPMAP ss16436727 Feb 27, 2004 (120)
7 PERLEGEN ss38338874 May 24, 2005 (125)
8 ABI ss43820922 Mar 15, 2006 (126)
9 ILLUMINA ss65729861 Oct 15, 2006 (127)
10 ILLUMINA ss66789648 Nov 30, 2006 (127)
11 ILLUMINA ss67880532 Nov 30, 2006 (127)
12 ILLUMINA ss68021762 Nov 30, 2006 (127)
13 ILLUMINA ss70974900 May 27, 2008 (130)
14 ILLUMINA ss71586393 May 17, 2007 (127)
15 ILLUMINA ss75780126 Dec 06, 2007 (129)
16 ILLUMINA ss79284165 Dec 16, 2007 (130)
17 KRIBB_YJKIM ss83579467 Dec 16, 2007 (130)
18 BCMHGSC_JDW ss87737982 Mar 23, 2008 (129)
19 BGI ss102777955 Dec 01, 2009 (131)
20 1000GENOMES ss108549523 Jan 23, 2009 (130)
21 1000GENOMES ss111059080 Jan 25, 2009 (130)
22 ILLUMINA ss122918884 Dec 01, 2009 (131)
23 ENSEMBL ss138066058 Dec 01, 2009 (131)
24 ILLUMINA ss154473975 Dec 01, 2009 (131)
25 GMI ss155577717 Dec 01, 2009 (131)
26 ILLUMINA ss159648469 Dec 01, 2009 (131)
27 ILLUMINA ss160957988 Dec 01, 2009 (131)
28 ENSEMBL ss161162361 Dec 01, 2009 (131)
29 COMPLETE_GENOMICS ss163963684 Jul 04, 2010 (132)
30 COMPLETE_GENOMICS ss165093642 Jul 04, 2010 (132)
31 ILLUMINA ss172410282 Jul 04, 2010 (132)
32 ILLUMINA ss174749202 Jul 04, 2010 (132)
33 BCM-HGSC-SUB ss205158626 Jul 04, 2010 (132)
34 1000GENOMES ss218615614 Jul 14, 2010 (132)
35 1000GENOMES ss230705718 Jul 14, 2010 (132)
36 1000GENOMES ss238359768 Jul 15, 2010 (132)
37 BL ss253410437 May 09, 2011 (134)
38 GMI ss275991446 May 04, 2012 (137)
39 GMI ss284127486 Apr 25, 2013 (138)
40 PJP ss290605924 May 09, 2011 (134)
41 ILLUMINA ss481808981 May 04, 2012 (137)
42 ILLUMINA ss481841472 May 04, 2012 (137)
43 ILLUMINA ss482802697 Sep 08, 2015 (146)
44 ILLUMINA ss485699171 May 04, 2012 (137)
45 ILLUMINA ss537565131 Sep 08, 2015 (146)
46 TISHKOFF ss554618549 Apr 25, 2013 (138)
47 SSMP ss648335856 Apr 25, 2013 (138)
48 ILLUMINA ss778629351 Sep 08, 2015 (146)
49 ILLUMINA ss783295142 Sep 08, 2015 (146)
50 ILLUMINA ss784247637 Sep 08, 2015 (146)
51 ILLUMINA ss825614683 Apr 01, 2015 (144)
52 ILLUMINA ss832556436 Sep 08, 2015 (146)
53 ILLUMINA ss833159290 Jul 12, 2019 (153)
54 ILLUMINA ss834086936 Sep 08, 2015 (146)
55 EVA-GONL ss975607632 Aug 21, 2014 (142)
56 JMKIDD_LAB ss1068219728 Aug 21, 2014 (142)
57 1000GENOMES ss1292573382 Aug 21, 2014 (142)
58 DDI ss1425947867 Apr 01, 2015 (144)
59 EVA_GENOME_DK ss1574346454 Apr 01, 2015 (144)
60 EVA_DECODE ss1584989701 Apr 01, 2015 (144)
61 EVA_UK10K_ALSPAC ss1601067219 Apr 01, 2015 (144)
62 EVA_UK10K_TWINSUK ss1644061252 Apr 01, 2015 (144)
63 EVA_MGP ss1710917556 Apr 01, 2015 (144)
64 EVA_SVP ss1712365976 Apr 01, 2015 (144)
65 ILLUMINA ss1751865735 Sep 08, 2015 (146)
66 WEILL_CORNELL_DGM ss1918806275 Feb 12, 2016 (147)
67 GENOMED ss1966849824 Jul 19, 2016 (147)
68 JJLAB ss2019928857 Sep 14, 2016 (149)
69 USC_VALOUEV ss2147947655 Dec 20, 2016 (150)
70 HUMAN_LONGEVITY ss2166008292 Dec 20, 2016 (150)
71 TOPMED ss2328375347 Dec 20, 2016 (150)
72 ILLUMINA ss2632567804 Nov 08, 2017 (151)
73 GRF ss2697877903 Nov 08, 2017 (151)
74 GNOMAD ss2759963029 Nov 08, 2017 (151)
75 AFFY ss2984872155 Nov 08, 2017 (151)
76 AFFY ss2985523429 Nov 08, 2017 (151)
77 SWEGEN ss2987496107 Nov 08, 2017 (151)
78 BIOINF_KMB_FNS_UNIBA ss3023728527 Nov 08, 2017 (151)
79 TOPMED ss3087730710 Nov 08, 2017 (151)
80 CSHL ss3343651802 Nov 08, 2017 (151)
81 ILLUMINA ss3626191300 Oct 11, 2018 (152)
82 ILLUMINA ss3630601230 Oct 11, 2018 (152)
83 ILLUMINA ss3632907547 Oct 11, 2018 (152)
84 ILLUMINA ss3633602743 Oct 11, 2018 (152)
85 ILLUMINA ss3634345134 Oct 11, 2018 (152)
86 ILLUMINA ss3635296265 Oct 11, 2018 (152)
87 ILLUMINA ss3636024626 Oct 11, 2018 (152)
88 ILLUMINA ss3637046735 Oct 11, 2018 (152)
89 ILLUMINA ss3637782417 Oct 11, 2018 (152)
90 ILLUMINA ss3638908969 Oct 11, 2018 (152)
91 ILLUMINA ss3639452615 Oct 11, 2018 (152)
92 ILLUMINA ss3640052493 Oct 11, 2018 (152)
93 ILLUMINA ss3642791973 Oct 11, 2018 (152)
94 ILLUMINA ss3651457571 Oct 11, 2018 (152)
95 ILLUMINA ss3653644246 Oct 11, 2018 (152)
96 EGCUT_WGS ss3655587170 Jul 12, 2019 (153)
97 EVA_DECODE ss3687600565 Jul 12, 2019 (153)
98 ACPOP ss3727419653 Jul 12, 2019 (153)
99 ILLUMINA ss3744646077 Jul 12, 2019 (153)
100 EVA ss3746715849 Jul 12, 2019 (153)
101 ILLUMINA ss3772147265 Jul 12, 2019 (153)
102 PACBIO ss3783529613 Jul 12, 2019 (153)
103 PACBIO ss3789169859 Jul 12, 2019 (153)
104 PACBIO ss3794042818 Jul 12, 2019 (153)
105 KHV_HUMAN_GENOMES ss3799717245 Jul 12, 2019 (153)
106 EVA ss3825572789 Apr 25, 2020 (154)
107 EVA ss3826388531 Apr 25, 2020 (154)
108 EVA ss3836585483 Apr 25, 2020 (154)
109 EVA ss3841994017 Apr 25, 2020 (154)
110 HGDP ss3847347575 Apr 25, 2020 (154)
111 SGDP_PRJ ss3849721534 Apr 25, 2020 (154)
112 KRGDB ss3894824530 Apr 25, 2020 (154)
113 KOGIC ss3945317125 Apr 25, 2020 (154)
114 FSA-LAB ss3983941831 Apr 25, 2021 (155)
115 EVA ss3984821663 Apr 25, 2021 (155)
116 EVA ss4016934063 Apr 25, 2021 (155)
117 TOPMED ss4464865973 Apr 25, 2021 (155)
118 TOMMO_GENOMICS ss5145838805 Apr 25, 2021 (155)
119 EVA ss5237163297 Apr 25, 2021 (155)
120 1000Genomes NC_000001.10 - 116948712 Oct 11, 2018 (152)
121 The Avon Longitudinal Study of Parents and Children NC_000001.10 - 116948712 Oct 11, 2018 (152)
122 Genetic variation in the Estonian population NC_000001.10 - 116948712 Oct 11, 2018 (152)
123 The Danish reference pan genome NC_000001.10 - 116948712 Apr 25, 2020 (154)
124 gnomAD - Genomes NC_000001.11 - 116406090 Apr 25, 2021 (155)
125 Genome of the Netherlands Release 5 NC_000001.10 - 116948712 Apr 25, 2020 (154)
126 HGDP-CEPH-db Supplement 1 NC_000001.9 - 116750235 Apr 25, 2020 (154)
127 HapMap NC_000001.11 - 116406090 Apr 25, 2020 (154)
128 KOREAN population from KRGDB NC_000001.10 - 116948712 Apr 25, 2020 (154)
129 Korean Genome Project NC_000001.11 - 116406090 Apr 25, 2020 (154)
130 Medical Genome Project healthy controls from Spanish population NC_000001.10 - 116948712 Apr 25, 2020 (154)
131 Northern Sweden NC_000001.10 - 116948712 Jul 12, 2019 (153)
132 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000001.10 - 116948712 Apr 25, 2021 (155)
133 Qatari NC_000001.10 - 116948712 Apr 25, 2020 (154)
134 SGDP_PRJ NC_000001.10 - 116948712 Apr 25, 2020 (154)
135 Siberian NC_000001.10 - 116948712 Apr 25, 2020 (154)
136 8.3KJPN NC_000001.10 - 116948712 Apr 25, 2021 (155)
137 TopMed NC_000001.11 - 116406090 Apr 25, 2021 (155)
138 UK 10K study - Twins NC_000001.10 - 116948712 Oct 11, 2018 (152)
139 A Vietnamese Genetic Variation Database NC_000001.10 - 116948712 Jul 12, 2019 (153)
140 ALFA NC_000001.11 - 116406090 Apr 25, 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)
rs61635763 May 27, 2008 (130)
rs117105687 Aug 16, 2010 (132)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss3638908969, ss3639452615 NC_000001.8:116660753:G:A NC_000001.11:116406089:G:A (self)
25467, ss87737982, ss108549523, ss111059080, ss163963684, ss165093642, ss205158626, ss253410437, ss275991446, ss284127486, ss290605924, ss481808981, ss825614683, ss1584989701, ss1712365976, ss3642791973, ss3847347575 NC_000001.9:116750234:G:A NC_000001.11:116406089:G:A (self)
3354211, 1858407, 1325418, 1679291, 808012, 2001924, 34308, 704518, 47590, 848205, 1738514, 464009, 3808112, 1858407, 401757, ss218615614, ss230705718, ss238359768, ss481841472, ss482802697, ss485699171, ss537565131, ss554618549, ss648335856, ss778629351, ss783295142, ss784247637, ss832556436, ss833159290, ss834086936, ss975607632, ss1068219728, ss1292573382, ss1425947867, ss1574346454, ss1601067219, ss1644061252, ss1710917556, ss1751865735, ss1918806275, ss1966849824, ss2019928857, ss2147947655, ss2328375347, ss2632567804, ss2697877903, ss2759963029, ss2984872155, ss2985523429, ss2987496107, ss3343651802, ss3626191300, ss3630601230, ss3632907547, ss3633602743, ss3634345134, ss3635296265, ss3636024626, ss3637046735, ss3637782417, ss3640052493, ss3651457571, ss3653644246, ss3655587170, ss3727419653, ss3744646077, ss3746715849, ss3772147265, ss3783529613, ss3789169859, ss3794042818, ss3825572789, ss3826388531, ss3836585483, ss3849721534, ss3894824530, ss3983941831, ss3984821663, ss4016934063, ss5145838805 NC_000001.10:116948711:G:A NC_000001.11:116406089:G:A (self)
23723001, 162206, 1695126, 17932730, 28472308, 4543385046, ss2166008292, ss3023728527, ss3087730710, ss3687600565, ss3799717245, ss3841994017, ss3945317125, ss4464865973, ss5237163297 NC_000001.11:116406089:G:A NC_000001.11:116406089:G:A (self)
ss16436727 NT_004754.15:864296:G:A NC_000001.11:116406089:G:A (self)
ss1221796, ss1647969, ss2733230, ss6683640, ss16253084, ss43820922, ss65729861, ss66789648, ss67880532, ss68021762, ss70974900, ss71586393, ss75780126, ss79284165, ss83579467, ss102777955, ss122918884, ss138066058, ss154473975, ss155577717, ss159648469, ss160957988, ss161162361, ss172410282, ss174749202 NT_032977.9:86920629:G:A NC_000001.11:116406089:G:A (self)
ss38338874, ss83579467 NT_032977.9:86920629:G:C NC_000001.11:116406089:G:C (self)
ss38338874, ss83579467 NT_032977.9:86920629:G:T NC_000001.11:116406089:G:T (self)
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Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

1 citation for rs850610
PMID Title Author Year Journal
18179887 Admixture mapping of white cell count: genetic locus responsible for lower white blood cell count in the Health ABC and Jackson Heart studies. Nalls MA et al. 2008 American journal of human genetics
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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.post596+ae089ad