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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.

rs10098

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr21:45295630 (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
A=0.487850 (129129/264690, TOPMED)
A=0.485003 (67880/139958, GnomAD)
G=0.451649 (50741/112346, ALFA) (+ 18 more)
G=0.42572 (12030/28258, 14KJPN)
G=0.42804 (7174/16760, 8.3KJPN)
A=0.4858 (3111/6404, 1000G_30x)
A=0.4876 (2442/5008, 1000G)
G=0.4013 (1798/4480, Estonian)
G=0.4450 (1715/3854, ALSPAC)
G=0.4409 (1635/3708, TWINSUK)
G=0.4515 (1323/2930, KOREAN)
G=0.4770 (994/2084, HGDP_Stanford)
A=0.4343 (820/1888, HapMap)
G=0.457 (456/998, GoNL)
G=0.437 (262/600, NorthernSweden)
G=0.282 (113/400, SGDP_PRJ)
A=0.472 (102/216, Qatari)
A=0.495 (107/216, Vietnamese)
G=0.41 (26/64, Ancient Sardinia)
G=0.33 (16/48, Siberian)
G=0.38 (15/40, GENOME_DK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
LINC00205 : Non Coding Transcript 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 112346 G=0.451649 A=0.548351
European Sub 88844 G=0.43626 A=0.56374
African Sub 6718 G=0.6957 A=0.3043
African Others Sub 246 G=0.780 A=0.220
African American Sub 6472 G=0.6925 A=0.3075
Asian Sub 534 G=0.427 A=0.573
East Asian Sub 452 G=0.403 A=0.597
Other Asian Sub 82 G=0.56 A=0.44
Latin American 1 Sub 696 G=0.520 A=0.480
Latin American 2 Sub 5620 G=0.3324 A=0.6676
South Asian Sub 5030 G=0.5060 A=0.4940
Other Sub 4904 G=0.4700 A=0.5300


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=0.512150 A=0.487850
gnomAD - Genomes Global Study-wide 139958 G=0.514997 A=0.485003
gnomAD - Genomes European Sub 75802 G=0.44007 A=0.55993
gnomAD - Genomes African Sub 41910 G=0.69699 A=0.30301
gnomAD - Genomes American Sub 13646 G=0.40481 A=0.59519
gnomAD - Genomes Ashkenazi Jewish Sub 3322 G=0.4332 A=0.5668
gnomAD - Genomes East Asian Sub 3128 G=0.4728 A=0.5272
gnomAD - Genomes Other Sub 2150 G=0.4963 A=0.5037
Allele Frequency Aggregator Total Global 112346 G=0.451649 A=0.548351
Allele Frequency Aggregator European Sub 88844 G=0.43626 A=0.56374
Allele Frequency Aggregator African Sub 6718 G=0.6957 A=0.3043
Allele Frequency Aggregator Latin American 2 Sub 5620 G=0.3324 A=0.6676
Allele Frequency Aggregator South Asian Sub 5030 G=0.5060 A=0.4940
Allele Frequency Aggregator Other Sub 4904 G=0.4700 A=0.5300
Allele Frequency Aggregator Latin American 1 Sub 696 G=0.520 A=0.480
Allele Frequency Aggregator Asian Sub 534 G=0.427 A=0.573
14KJPN JAPANESE Study-wide 28258 G=0.42572 A=0.57428
8.3KJPN JAPANESE Study-wide 16760 G=0.42804 A=0.57196
1000Genomes_30x Global Study-wide 6404 G=0.5142 A=0.4858
1000Genomes_30x African Sub 1786 G=0.7413 A=0.2587
1000Genomes_30x Europe Sub 1266 G=0.4329 A=0.5671
1000Genomes_30x South Asian Sub 1202 G=0.4809 A=0.5191
1000Genomes_30x East Asian Sub 1170 G=0.4513 A=0.5487
1000Genomes_30x American Sub 980 G=0.321 A=0.679
1000Genomes Global Study-wide 5008 G=0.5124 A=0.4876
1000Genomes African Sub 1322 G=0.7390 A=0.2610
1000Genomes East Asian Sub 1008 G=0.4544 A=0.5456
1000Genomes Europe Sub 1006 G=0.4354 A=0.5646
1000Genomes South Asian Sub 978 G=0.472 A=0.528
1000Genomes American Sub 694 G=0.333 A=0.667
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.4013 A=0.5987
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.4450 A=0.5550
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.4409 A=0.5591
KOREAN population from KRGDB KOREAN Study-wide 2930 G=0.4515 A=0.5485, C=0.0000
HGDP-CEPH-db Supplement 1 Global Study-wide 2084 G=0.4770 A=0.5230
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 G=0.434 A=0.566
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 G=0.570 A=0.430
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 G=0.491 A=0.509
HGDP-CEPH-db Supplement 1 Europe Sub 320 G=0.434 A=0.566
HGDP-CEPH-db Supplement 1 Africa Sub 242 G=0.736 A=0.264
HGDP-CEPH-db Supplement 1 America Sub 216 G=0.167 A=0.833
HGDP-CEPH-db Supplement 1 Oceania Sub 72 G=0.40 A=0.60
HapMap Global Study-wide 1888 G=0.5657 A=0.4343
HapMap American Sub 766 G=0.432 A=0.568
HapMap African Sub 692 G=0.763 A=0.237
HapMap Asian Sub 254 G=0.453 A=0.547
HapMap Europe Sub 176 G=0.534 A=0.466
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.457 A=0.543
Northern Sweden ACPOP Study-wide 600 G=0.437 A=0.563
SGDP_PRJ Global Study-wide 400 G=0.282 A=0.718
Qatari Global Study-wide 216 G=0.528 A=0.472
A Vietnamese Genetic Variation Database Global Study-wide 216 G=0.505 A=0.495
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 64 G=0.41 A=0.59
Siberian Global Study-wide 48 G=0.33 A=0.67
The Danish reference pan genome Danish Study-wide 40 G=0.38 A=0.62
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 21 NC_000021.9:g.45295630G>A
GRCh38.p14 chr 21 NC_000021.9:g.45295630G>C
GRCh37.p13 chr 21 NC_000021.8:g.46715545G>A
GRCh37.p13 chr 21 NC_000021.8:g.46715545G>C
Gene: LINC00205, long intergenic non-protein coding RNA 205 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
LINC00205 transcript NR_026943.1:n.5441G>A N/A Non Coding Transcript Variant
LINC00205 transcript NR_026943.1:n.5441G>C N/A Non Coding 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 21 NC_000021.9:g.45295630= NC_000021.9:g.45295630G>A NC_000021.9:g.45295630G>C
GRCh37.p13 chr 21 NC_000021.8:g.46715545= NC_000021.8:g.46715545G>A NC_000021.8:g.46715545G>C
LINC00205 transcript NR_026943.1:n.5441= NR_026943.1:n.5441G>A NR_026943.1:n.5441G>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#.

123 SubSNP, 21 Frequency submissions
No Submitter Submission ID Date (Build)
1 CGAP-GAI ss12239 Sep 19, 2000 (52)
2 LEE ss1539566 Oct 04, 2000 (86)
3 PERLEGEN ss4019843 Sep 28, 2001 (100)
4 LEE ss4398616 May 29, 2002 (106)
5 LEE ss4426946 May 29, 2002 (106)
6 WUGSC_SSAHASNP ss14443954 Dec 05, 2003 (119)
7 CGAP-GAI ss16228956 Feb 27, 2004 (120)
8 SSAHASNP ss21817072 Apr 05, 2004 (121)
9 PERLEGEN ss24526669 Sep 20, 2004 (123)
10 ABI ss44279232 Mar 14, 2006 (126)
11 ILLUMINA ss65714097 Oct 16, 2006 (127)
12 ILLUMINA ss66631765 Dec 01, 2006 (127)
13 ILLUMINA ss66869400 Dec 01, 2006 (127)
14 ILLUMINA ss66945118 Dec 01, 2006 (127)
15 PERLEGEN ss69256125 May 17, 2007 (127)
16 ILLUMINA ss70358691 May 17, 2007 (127)
17 ILLUMINA ss70464851 May 26, 2008 (130)
18 ILLUMINA ss70986003 May 17, 2007 (127)
19 AFFY ss74839546 Aug 16, 2007 (128)
20 ILLUMINA ss75497613 Dec 06, 2007 (129)
21 HGSV ss77162866 Dec 06, 2007 (129)
22 KRIBB_YJKIM ss83349421 Dec 15, 2007 (130)
23 HUMANGENOME_JCVI ss96152418 Feb 06, 2009 (130)
24 BGI ss106216958 Feb 06, 2009 (130)
25 1000GENOMES ss112525929 Jan 25, 2009 (130)
26 CHURCH_CG54K ss120035015 Dec 01, 2009 (131)
27 ILLUMINA ss120241574 Dec 01, 2009 (131)
28 ILLUMINA ss121264042 Dec 01, 2009 (131)
29 ENSEMBL ss135588425 Dec 01, 2009 (131)
30 ILLUMINA ss152568045 Dec 01, 2009 (131)
31 GMI ss156973800 Dec 01, 2009 (131)
32 ILLUMINA ss159108810 Dec 01, 2009 (131)
33 ILLUMINA ss159862991 Dec 01, 2009 (131)
34 COMPLETE_GENOMICS ss168166198 Jul 04, 2010 (132)
35 ILLUMINA ss169257477 Jul 04, 2010 (132)
36 ILLUMINA ss169662966 Jul 04, 2010 (132)
37 COMPLETE_GENOMICS ss172104421 Jul 04, 2010 (132)
38 BUSHMAN ss204038116 Jul 04, 2010 (132)
39 BCM-HGSC-SUB ss208768720 Jul 04, 2010 (132)
40 1000GENOMES ss228600549 Jul 14, 2010 (132)
41 1000GENOMES ss238008148 Jul 15, 2010 (132)
42 1000GENOMES ss244141211 Jul 15, 2010 (132)
43 ILLUMINA ss244260744 Jul 04, 2010 (132)
44 BL ss256014548 May 09, 2011 (134)
45 GMI ss283565021 May 04, 2012 (137)
46 GMI ss287542376 Apr 25, 2013 (138)
47 PJP ss292662442 May 09, 2011 (134)
48 ILLUMINA ss479518399 Sep 08, 2015 (146)
49 ILLUMINA ss483950679 May 04, 2012 (137)
50 ILLUMINA ss484282581 May 04, 2012 (137)
51 ILLUMINA ss536144648 Sep 08, 2015 (146)
52 TISHKOFF ss566538782 Apr 25, 2013 (138)
53 SSMP ss662450605 Apr 25, 2013 (138)
54 ILLUMINA ss779521296 Sep 08, 2015 (146)
55 ILLUMINA ss782419253 Sep 08, 2015 (146)
56 ILLUMINA ss825328422 Apr 01, 2015 (144)
57 ILLUMINA ss832621580 Jul 13, 2019 (153)
58 ILLUMINA ss834991771 Sep 08, 2015 (146)
59 EVA-GONL ss995184169 Aug 21, 2014 (142)
60 JMKIDD_LAB ss1082547217 Aug 21, 2014 (142)
61 1000GENOMES ss1366531969 Aug 21, 2014 (142)
62 DDI ss1429204708 Apr 01, 2015 (144)
63 EVA_GENOME_DK ss1579688895 Apr 01, 2015 (144)
64 EVA_UK10K_ALSPAC ss1639690752 Apr 01, 2015 (144)
65 EVA_UK10K_TWINSUK ss1682684785 Apr 01, 2015 (144)
66 EVA_DECODE ss1699255398 Apr 01, 2015 (144)
67 EVA_SVP ss1713728677 Apr 01, 2015 (144)
68 HAMMER_LAB ss1809718150 Sep 08, 2015 (146)
69 WEILL_CORNELL_DGM ss1938736396 Feb 12, 2016 (147)
70 GENOMED ss1969239655 Jul 19, 2016 (147)
71 JJLAB ss2030142976 Sep 14, 2016 (149)
72 USC_VALOUEV ss2158749068 Dec 20, 2016 (150)
73 HUMAN_LONGEVITY ss2246235106 Dec 20, 2016 (150)
74 SYSTEMSBIOZJU ss2629570643 Nov 08, 2017 (151)
75 ILLUMINA ss2633858246 Nov 08, 2017 (151)
76 GRF ss2704480075 Nov 08, 2017 (151)
77 GNOMAD ss2972461709 Nov 08, 2017 (151)
78 SWEGEN ss3018992741 Nov 08, 2017 (151)
79 BIOINF_KMB_FNS_UNIBA ss3028910194 Nov 08, 2017 (151)
80 CSHL ss3352750047 Nov 08, 2017 (151)
81 ILLUMINA ss3628497658 Oct 12, 2018 (152)
82 ILLUMINA ss3631811114 Oct 12, 2018 (152)
83 ILLUMINA ss3636554495 Oct 12, 2018 (152)
84 ILLUMINA ss3638372109 Oct 12, 2018 (152)
85 ILLUMINA ss3639190082 Oct 12, 2018 (152)
86 ILLUMINA ss3639611003 Oct 12, 2018 (152)
87 ILLUMINA ss3641135284 Oct 12, 2018 (152)
88 ILLUMINA ss3641431625 Oct 12, 2018 (152)
89 ILLUMINA ss3643332727 Oct 12, 2018 (152)
90 OMUKHERJEE_ADBS ss3646558154 Oct 12, 2018 (152)
91 URBANLAB ss3651129762 Oct 12, 2018 (152)
92 EGCUT_WGS ss3685568679 Jul 13, 2019 (153)
93 EVA_DECODE ss3707851574 Jul 13, 2019 (153)
94 ACPOP ss3743787767 Jul 13, 2019 (153)
95 EVA ss3759186398 Jul 13, 2019 (153)
96 PACBIO ss3788781287 Jul 13, 2019 (153)
97 PACBIO ss3793653506 Jul 13, 2019 (153)
98 PACBIO ss3798539819 Jul 13, 2019 (153)
99 KHV_HUMAN_GENOMES ss3822350264 Jul 13, 2019 (153)
100 EVA ss3835908133 Apr 27, 2020 (154)
101 EVA ss3841582059 Apr 27, 2020 (154)
102 EVA ss3847094905 Apr 27, 2020 (154)
103 HGDP ss3847683580 Apr 27, 2020 (154)
104 SGDP_PRJ ss3890140793 Apr 27, 2020 (154)
105 KRGDB ss3940491991 Apr 27, 2020 (154)
106 FSA-LAB ss3984227615 Apr 26, 2021 (155)
107 EVA ss3985908236 Apr 26, 2021 (155)
108 EVA ss3986086357 Apr 26, 2021 (155)
109 EVA ss4017871794 Apr 26, 2021 (155)
110 TOPMED ss5103498249 Apr 26, 2021 (155)
111 TOMMO_GENOMICS ss5231807433 Apr 26, 2021 (155)
112 1000G_HIGH_COVERAGE ss5310421514 Oct 16, 2022 (156)
113 EVA ss5316044025 Oct 16, 2022 (156)
114 EVA ss5440283675 Oct 16, 2022 (156)
115 HUGCELL_USP ss5502447132 Oct 16, 2022 (156)
116 1000G_HIGH_COVERAGE ss5617655156 Oct 16, 2022 (156)
117 SANFORD_IMAGENETICS ss5664139115 Oct 16, 2022 (156)
118 TOMMO_GENOMICS ss5792386775 Oct 16, 2022 (156)
119 YY_MCH ss5818495666 Oct 16, 2022 (156)
120 EVA ss5839129580 Oct 16, 2022 (156)
121 EVA ss5853331054 Oct 16, 2022 (156)
122 EVA ss5892589846 Oct 16, 2022 (156)
123 EVA ss5959038850 Oct 16, 2022 (156)
124 1000Genomes NC_000021.8 - 46715545 Oct 12, 2018 (152)
125 1000Genomes_30x NC_000021.9 - 45295630 Oct 16, 2022 (156)
126 The Avon Longitudinal Study of Parents and Children NC_000021.8 - 46715545 Oct 12, 2018 (152)
127 Genetic variation in the Estonian population NC_000021.8 - 46715545 Oct 12, 2018 (152)
128 The Danish reference pan genome NC_000021.8 - 46715545 Apr 27, 2020 (154)
129 gnomAD - Genomes NC_000021.9 - 45295630 Apr 26, 2021 (155)
130 Genome of the Netherlands Release 5 NC_000021.8 - 46715545 Apr 27, 2020 (154)
131 HGDP-CEPH-db Supplement 1 NC_000021.7 - 45539973 Apr 27, 2020 (154)
132 HapMap NC_000021.9 - 45295630 Apr 27, 2020 (154)
133 KOREAN population from KRGDB NC_000021.8 - 46715545 Apr 27, 2020 (154)
134 Northern Sweden NC_000021.8 - 46715545 Jul 13, 2019 (153)
135 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000021.8 - 46715545 Apr 26, 2021 (155)
136 Qatari NC_000021.8 - 46715545 Apr 27, 2020 (154)
137 SGDP_PRJ NC_000021.8 - 46715545 Apr 27, 2020 (154)
138 Siberian NC_000021.8 - 46715545 Apr 27, 2020 (154)
139 8.3KJPN NC_000021.8 - 46715545 Apr 26, 2021 (155)
140 14KJPN NC_000021.9 - 45295630 Oct 16, 2022 (156)
141 TopMed NC_000021.9 - 45295630 Apr 26, 2021 (155)
142 UK 10K study - Twins NC_000021.8 - 46715545 Oct 12, 2018 (152)
143 A Vietnamese Genetic Variation Database NC_000021.8 - 46715545 Jul 13, 2019 (153)
144 ALFA NC_000021.9 - 45295630 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)
rs3171493 Jul 03, 2002 (106)
rs17250477 Oct 07, 2004 (123)
rs52800204 Sep 21, 2007 (128)
rs61031723 May 26, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
361472, ss77162866, ss112525929, ss168166198, ss172104421, ss204038116, ss208768720, ss256014548, ss283565021, ss287542376, ss292662442, ss484282581, ss825328422, ss1699255398, ss1713728677, ss3639190082, ss3639611003, ss3643332727, ss3847683580 NC_000021.7:45539972:G:A NC_000021.9:45295629:G:A (self)
80060907, 44311464, 31306927, 5853834, 19738950, 47669385, 17072632, 1134163, 20778318, 42157773, 11265422, 89776740, 44311464, 9776635, ss228600549, ss238008148, ss244141211, ss479518399, ss483950679, ss536144648, ss566538782, ss662450605, ss779521296, ss782419253, ss832621580, ss834991771, ss995184169, ss1082547217, ss1366531969, ss1429204708, ss1579688895, ss1639690752, ss1682684785, ss1809718150, ss1938736396, ss1969239655, ss2030142976, ss2158749068, ss2629570643, ss2633858246, ss2704480075, ss2972461709, ss3018992741, ss3352750047, ss3628497658, ss3631811114, ss3636554495, ss3638372109, ss3641135284, ss3641431625, ss3646558154, ss3685568679, ss3743787767, ss3759186398, ss3788781287, ss3793653506, ss3798539819, ss3835908133, ss3841582059, ss3890140793, ss3940491991, ss3984227615, ss3985908236, ss3986086357, ss4017871794, ss5231807433, ss5316044025, ss5440283675, ss5664139115, ss5839129580, ss5959038850 NC_000021.8:46715544:G:A NC_000021.9:45295629:G:A (self)
105181091, 564755859, 2221604, 126223879, 378607195, 5521654692, ss2246235106, ss3028910194, ss3651129762, ss3707851574, ss3822350264, ss3847094905, ss5103498249, ss5310421514, ss5502447132, ss5617655156, ss5792386775, ss5818495666, ss5853331054, ss5892589846 NC_000021.9:45295629:G:A NC_000021.9:45295629:G:A (self)
ss14443954, ss21817072 NT_011515.10:2028282:G:A NC_000021.9:45295629:G:A (self)
ss12239, ss1539566, ss4019843, ss4398616, ss4426946, ss16228956, ss24526669, ss44279232, ss65714097, ss66631765, ss66869400, ss66945118, ss69256125, ss70358691, ss70464851, ss70986003, ss74839546, ss75497613, ss83349421, ss96152418, ss106216958, ss120035015, ss120241574, ss121264042, ss135588425, ss152568045, ss156973800, ss159108810, ss159862991, ss169257477, ss169662966, ss244260744 NT_011515.12:3709985:G:A NC_000021.9:45295629:G:A (self)
47669385, ss3940491991 NC_000021.8:46715544:G:C NC_000021.9:45295629: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 rs10098

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