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.

rs1395821

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr4:147126398 (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=0.305788 (80939/264690, TOPMED)
C=0.212586 (48186/226666, ALFA)
C=0.301809 (42208/139850, GnomAD) (+ 20 more)
C=0.37782 (29734/78698, PAGE_STUDY)
C=0.41252 (11657/28258, 14KJPN)
C=0.40943 (6862/16760, 8.3KJPN)
C=0.3705 (2373/6404, 1000G_30x)
C=0.3674 (1840/5008, 1000G)
C=0.2598 (1164/4480, Estonian)
C=0.1759 (678/3854, ALSPAC)
C=0.1810 (671/3708, TWINSUK)
C=0.3587 (1051/2930, KOREAN)
C=0.3647 (760/2084, HGDP_Stanford)
C=0.3547 (671/1892, HapMap)
C=0.183 (183/998, GoNL)
C=0.346 (273/790, PRJEB37584)
C=0.223 (134/600, NorthernSweden)
C=0.244 (114/468, SGDP_PRJ)
C=0.329 (71/216, Qatari)
C=0.383 (82/214, Vietnamese)
C=0.10 (6/58, Ancient Sardinia)
C=0.26 (14/54, Siberian)
C=0.20 (8/40, GENOME_DK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
None
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 226760 C=0.212626 T=0.787374
European Sub 196076 C=0.192104 T=0.807896
African Sub 5920 C=0.5341 T=0.4659
African Others Sub 224 C=0.598 T=0.402
African American Sub 5696 C=0.5316 T=0.4684
Asian Sub 6370 C=0.3567 T=0.6433
East Asian Sub 4536 C=0.3560 T=0.6440
Other Asian Sub 1834 C=0.3582 T=0.6418
Latin American 1 Sub 550 C=0.242 T=0.758
Latin American 2 Sub 1572 C=0.1940 T=0.8060
South Asian Sub 5138 C=0.3595 T=0.6405
Other Sub 11134 C=0.25409 T=0.74591


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=0.305788 T=0.694212
Allele Frequency Aggregator Total Global 226666 C=0.212586 T=0.787414
Allele Frequency Aggregator European Sub 196000 C=0.192061 T=0.807939
Allele Frequency Aggregator Other Sub 11116 C=0.25396 T=0.74604
Allele Frequency Aggregator Asian Sub 6370 C=0.3567 T=0.6433
Allele Frequency Aggregator African Sub 5920 C=0.5341 T=0.4659
Allele Frequency Aggregator South Asian Sub 5138 C=0.3595 T=0.6405
Allele Frequency Aggregator Latin American 2 Sub 1572 C=0.1940 T=0.8060
Allele Frequency Aggregator Latin American 1 Sub 550 C=0.242 T=0.758
gnomAD - Genomes Global Study-wide 139850 C=0.301809 T=0.698191
gnomAD - Genomes European Sub 75846 C=0.19830 T=0.80170
gnomAD - Genomes African Sub 41764 C=0.52059 T=0.47941
gnomAD - Genomes American Sub 13640 C=0.21525 T=0.78475
gnomAD - Genomes Ashkenazi Jewish Sub 3322 C=0.2182 T=0.7818
gnomAD - Genomes East Asian Sub 3124 C=0.3604 T=0.6396
gnomAD - Genomes Other Sub 2154 C=0.2967 T=0.7033
The PAGE Study Global Study-wide 78698 C=0.37782 T=0.62218
The PAGE Study AfricanAmerican Sub 32514 C=0.50658 T=0.49342
The PAGE Study Mexican Sub 10808 C=0.21392 T=0.78608
The PAGE Study Asian Sub 8318 C=0.4005 T=0.5995
The PAGE Study PuertoRican Sub 7918 C=0.2778 T=0.7222
The PAGE Study NativeHawaiian Sub 4534 C=0.3092 T=0.6908
The PAGE Study Cuban Sub 4230 C=0.2520 T=0.7480
The PAGE Study Dominican Sub 3828 C=0.3495 T=0.6505
The PAGE Study CentralAmerican Sub 2450 C=0.2429 T=0.7571
The PAGE Study SouthAmerican Sub 1982 C=0.2205 T=0.7795
The PAGE Study NativeAmerican Sub 1260 C=0.2230 T=0.7770
The PAGE Study SouthAsian Sub 856 C=0.352 T=0.648
14KJPN JAPANESE Study-wide 28258 C=0.41252 T=0.58748
8.3KJPN JAPANESE Study-wide 16760 C=0.40943 T=0.59057
1000Genomes_30x Global Study-wide 6404 C=0.3705 T=0.6295
1000Genomes_30x African Sub 1786 C=0.5733 T=0.4267
1000Genomes_30x Europe Sub 1266 C=0.1951 T=0.8049
1000Genomes_30x South Asian Sub 1202 C=0.3794 T=0.6206
1000Genomes_30x East Asian Sub 1170 C=0.3718 T=0.6282
1000Genomes_30x American Sub 980 C=0.215 T=0.785
1000Genomes Global Study-wide 5008 C=0.3674 T=0.6326
1000Genomes African Sub 1322 C=0.5651 T=0.4349
1000Genomes East Asian Sub 1008 C=0.3700 T=0.6300
1000Genomes Europe Sub 1006 C=0.1998 T=0.8002
1000Genomes South Asian Sub 978 C=0.375 T=0.625
1000Genomes American Sub 694 C=0.219 T=0.781
Genetic variation in the Estonian population Estonian Study-wide 4480 C=0.2598 T=0.7402
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 C=0.1759 T=0.8241
UK 10K study - Twins TWIN COHORT Study-wide 3708 C=0.1810 T=0.8190
KOREAN population from KRGDB KOREAN Study-wide 2930 C=0.3587 A=0.0000, G=0.0000, T=0.6413
HGDP-CEPH-db Supplement 1 Global Study-wide 2084 C=0.3647 T=0.6353
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 C=0.402 T=0.598
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 C=0.394 T=0.606
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 C=0.274 T=0.726
HGDP-CEPH-db Supplement 1 Europe Sub 320 C=0.216 T=0.784
HGDP-CEPH-db Supplement 1 Africa Sub 242 C=0.736 T=0.264
HGDP-CEPH-db Supplement 1 America Sub 216 C=0.218 T=0.782
HGDP-CEPH-db Supplement 1 Oceania Sub 72 C=0.25 T=0.75
HapMap Global Study-wide 1892 C=0.3547 T=0.6453
HapMap American Sub 770 C=0.310 T=0.690
HapMap African Sub 692 C=0.442 T=0.558
HapMap Asian Sub 254 C=0.374 T=0.626
HapMap Europe Sub 176 C=0.176 T=0.824
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 C=0.183 T=0.817
CNV burdens in cranial meningiomas Global Study-wide 790 C=0.346 T=0.654
CNV burdens in cranial meningiomas CRM Sub 790 C=0.346 T=0.654
Northern Sweden ACPOP Study-wide 600 C=0.223 T=0.777
SGDP_PRJ Global Study-wide 468 C=0.244 T=0.756
Qatari Global Study-wide 216 C=0.329 T=0.671
A Vietnamese Genetic Variation Database Global Study-wide 214 C=0.383 T=0.617
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 58 C=0.10 T=0.90
Siberian Global Study-wide 54 C=0.26 T=0.74
The Danish reference pan genome Danish Study-wide 40 C=0.20 T=0.80
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.147126398C>A
GRCh38.p14 chr 4 NC_000004.12:g.147126398C>G
GRCh38.p14 chr 4 NC_000004.12:g.147126398C>T
GRCh37.p13 chr 4 NC_000004.11:g.148047550C>A
GRCh37.p13 chr 4 NC_000004.11:g.148047550C>G
GRCh37.p13 chr 4 NC_000004.11:g.148047550C>T
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 4 NC_000004.12:g.147126398= NC_000004.12:g.147126398C>A NC_000004.12:g.147126398C>G NC_000004.12:g.147126398C>T
GRCh37.p13 chr 4 NC_000004.11:g.148047550= NC_000004.11:g.148047550C>A NC_000004.11:g.148047550C>G NC_000004.11:g.148047550C>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#.

124 SubSNP, 23 Frequency submissions
No Submitter Submission ID Date (Build)
1 TSC-CSHL ss2191491 Oct 23, 2000 (88)
2 CSHL-HAPMAP ss17013827 Feb 27, 2004 (120)
3 SSAHASNP ss22176088 Apr 05, 2004 (121)
4 PERLEGEN ss24153794 Sep 20, 2004 (123)
5 SEQUENOM ss24782131 Sep 21, 2004 (123)
6 SSAHASNP ss35361839 May 24, 2005 (125)
7 ABI ss44521864 Mar 13, 2006 (126)
8 ILLUMINA ss67094565 Dec 01, 2006 (127)
9 ILLUMINA ss67429017 Dec 01, 2006 (127)
10 ILLUMINA ss68153585 Dec 12, 2006 (127)
11 ILLUMINA ss70613059 May 25, 2008 (130)
12 ILLUMINA ss71160731 May 17, 2007 (127)
13 ILLUMINA ss75764257 Dec 07, 2007 (129)
14 KRIBB_YJKIM ss83753809 Dec 15, 2007 (130)
15 BCMHGSC_JDW ss92820740 Mar 24, 2008 (129)
16 HUMANGENOME_JCVI ss98872579 Feb 05, 2009 (130)
17 BGI ss104127928 Dec 01, 2009 (131)
18 1000GENOMES ss108435411 Jan 23, 2009 (130)
19 1000GENOMES ss110764814 Jan 25, 2009 (130)
20 ENSEMBL ss135100693 Dec 01, 2009 (131)
21 ENSEMBL ss139947037 Dec 01, 2009 (131)
22 ILLUMINA ss153412140 Dec 01, 2009 (131)
23 GMI ss158036866 Dec 01, 2009 (131)
24 ILLUMINA ss159264736 Dec 01, 2009 (131)
25 COMPLETE_GENOMICS ss162639342 Jul 04, 2010 (132)
26 COMPLETE_GENOMICS ss164647309 Jul 04, 2010 (132)
27 COMPLETE_GENOMICS ss167273848 Jul 04, 2010 (132)
28 ILLUMINA ss172469698 Jul 04, 2010 (132)
29 BUSHMAN ss199318358 Jul 04, 2010 (132)
30 BCM-HGSC-SUB ss206325579 Jul 04, 2010 (132)
31 1000GENOMES ss221277158 Jul 14, 2010 (132)
32 1000GENOMES ss232645979 Jul 14, 2010 (132)
33 1000GENOMES ss239883189 Jul 15, 2010 (132)
34 BL ss253607197 May 09, 2011 (134)
35 GMI ss277981108 May 04, 2012 (137)
36 GMI ss285027752 Apr 25, 2013 (138)
37 PJP ss293220745 May 09, 2011 (134)
38 EXOME_CHIP ss491361225 May 04, 2012 (137)
39 ILLUMINA ss536864285 Sep 08, 2015 (146)
40 TISHKOFF ss557930223 Apr 25, 2013 (138)
41 SSMP ss651750640 Apr 25, 2013 (138)
42 ILLUMINA ss780681893 Sep 08, 2015 (146)
43 ILLUMINA ss783355225 Sep 08, 2015 (146)
44 ILLUMINA ss832776938 Jul 13, 2019 (153)
45 EVA-GONL ss980807008 Aug 21, 2014 (142)
46 JMKIDD_LAB ss1072053247 Aug 21, 2014 (142)
47 1000GENOMES ss1312301238 Aug 21, 2014 (142)
48 DDI ss1430090741 Apr 01, 2015 (144)
49 EVA_GENOME_DK ss1580827246 Apr 01, 2015 (144)
50 EVA_DECODE ss1590319502 Apr 01, 2015 (144)
51 EVA_UK10K_ALSPAC ss1611425260 Apr 01, 2015 (144)
52 EVA_UK10K_TWINSUK ss1654419293 Apr 01, 2015 (144)
53 EVA_SVP ss1712714214 Apr 01, 2015 (144)
54 ILLUMINA ss1752501949 Sep 08, 2015 (146)
55 ILLUMINA ss1917785199 Feb 12, 2016 (147)
56 WEILL_CORNELL_DGM ss1924048646 Feb 12, 2016 (147)
57 ILLUMINA ss1946129408 Feb 12, 2016 (147)
58 ILLUMINA ss1958728172 Feb 12, 2016 (147)
59 GENOMED ss1969900926 Jul 19, 2016 (147)
60 JJLAB ss2022610304 Sep 14, 2016 (149)
61 USC_VALOUEV ss2150741965 Dec 20, 2016 (150)
62 HUMAN_LONGEVITY ss2268129014 Dec 20, 2016 (150)
63 SYSTEMSBIOZJU ss2625801273 Nov 08, 2017 (151)
64 ILLUMINA ss2635137754 Nov 08, 2017 (151)
65 GRF ss2706237426 Nov 08, 2017 (151)
66 GNOMAD ss2816657826 Nov 08, 2017 (151)
67 AFFY ss2985305703 Nov 08, 2017 (151)
68 AFFY ss2985932767 Nov 08, 2017 (151)
69 SWEGEN ss2995752713 Nov 08, 2017 (151)
70 ILLUMINA ss3022424387 Nov 08, 2017 (151)
71 BIOINF_KMB_FNS_UNIBA ss3025082033 Nov 08, 2017 (151)
72 CSHL ss3346018164 Nov 08, 2017 (151)
73 ILLUMINA ss3629088534 Oct 12, 2018 (152)
74 ILLUMINA ss3629088535 Oct 12, 2018 (152)
75 ILLUMINA ss3634974609 Oct 12, 2018 (152)
76 ILLUMINA ss3638517427 Oct 12, 2018 (152)
77 ILLUMINA ss3639260858 Oct 12, 2018 (152)
78 ILLUMINA ss3639928668 Oct 12, 2018 (152)
79 ILLUMINA ss3640681903 Oct 12, 2018 (152)
80 ILLUMINA ss3643466382 Oct 12, 2018 (152)
81 ILLUMINA ss3643974615 Oct 12, 2018 (152)
82 ILLUMINA ss3644862246 Oct 12, 2018 (152)
83 URBANLAB ss3647878181 Oct 12, 2018 (152)
84 ILLUMINA ss3652914536 Oct 12, 2018 (152)
85 ILLUMINA ss3654077657 Oct 12, 2018 (152)
86 EGCUT_WGS ss3663658360 Jul 13, 2019 (153)
87 EVA_DECODE ss3713294722 Jul 13, 2019 (153)
88 ILLUMINA ss3726179023 Jul 13, 2019 (153)
89 ACPOP ss3731713214 Jul 13, 2019 (153)
90 ILLUMINA ss3744530394 Jul 13, 2019 (153)
91 ILLUMINA ss3745274828 Jul 13, 2019 (153)
92 EVA ss3762558004 Jul 13, 2019 (153)
93 PAGE_CC ss3771159837 Jul 13, 2019 (153)
94 ILLUMINA ss3772769285 Jul 13, 2019 (153)
95 PACBIO ss3784896029 Jul 13, 2019 (153)
96 PACBIO ss3790327415 Jul 13, 2019 (153)
97 PACBIO ss3795202968 Jul 13, 2019 (153)
98 KHV_HUMAN_GENOMES ss3805719662 Jul 13, 2019 (153)
99 EVA ss3828869931 Apr 26, 2020 (154)
100 EVA ss3837885460 Apr 26, 2020 (154)
101 EVA ss3843325584 Apr 26, 2020 (154)
102 HGDP ss3847768165 Apr 26, 2020 (154)
103 SGDP_PRJ ss3860312842 Apr 26, 2020 (154)
104 KRGDB ss3906650645 Apr 26, 2020 (154)
105 EVA ss3984536592 Apr 26, 2021 (155)
106 EVA ss3985101584 Apr 26, 2021 (155)
107 EVA ss4017173820 Apr 26, 2021 (155)
108 TOPMED ss4636256353 Apr 26, 2021 (155)
109 TOMMO_GENOMICS ss5168553581 Apr 26, 2021 (155)
110 1000G_HIGH_COVERAGE ss5261447503 Oct 17, 2022 (156)
111 EVA ss5314998380 Oct 17, 2022 (156)
112 EVA ss5353072012 Oct 17, 2022 (156)
113 HUGCELL_USP ss5459956141 Oct 17, 2022 (156)
114 EVA ss5507776761 Oct 17, 2022 (156)
115 1000G_HIGH_COVERAGE ss5543769459 Oct 17, 2022 (156)
116 SANFORD_IMAGENETICS ss5624570321 Oct 17, 2022 (156)
117 SANFORD_IMAGENETICS ss5636344511 Oct 17, 2022 (156)
118 TOMMO_GENOMICS ss5703696370 Oct 17, 2022 (156)
119 YY_MCH ss5805643372 Oct 17, 2022 (156)
120 EVA ss5844880334 Oct 17, 2022 (156)
121 EVA ss5848027945 Oct 17, 2022 (156)
122 EVA ss5854495868 Oct 17, 2022 (156)
123 EVA ss5865986539 Oct 17, 2022 (156)
124 EVA ss5964747664 Oct 17, 2022 (156)
125 1000Genomes NC_000004.11 - 148047550 Oct 12, 2018 (152)
126 1000Genomes_30x NC_000004.12 - 147126398 Oct 17, 2022 (156)
127 The Avon Longitudinal Study of Parents and Children NC_000004.11 - 148047550 Oct 12, 2018 (152)
128 Genetic variation in the Estonian population NC_000004.11 - 148047550 Oct 12, 2018 (152)
129 The Danish reference pan genome NC_000004.11 - 148047550 Apr 26, 2020 (154)
130 gnomAD - Genomes NC_000004.12 - 147126398 Apr 26, 2021 (155)
131 Genome of the Netherlands Release 5 NC_000004.11 - 148047550 Apr 26, 2020 (154)
132 HGDP-CEPH-db Supplement 1 NC_000004.10 - 148267000 Apr 26, 2020 (154)
133 HapMap NC_000004.12 - 147126398 Apr 26, 2020 (154)
134 KOREAN population from KRGDB NC_000004.11 - 148047550 Apr 26, 2020 (154)
135 Northern Sweden NC_000004.11 - 148047550 Jul 13, 2019 (153)
136 The PAGE Study NC_000004.12 - 147126398 Jul 13, 2019 (153)
137 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000004.11 - 148047550 Apr 26, 2021 (155)
138 CNV burdens in cranial meningiomas NC_000004.11 - 148047550 Apr 26, 2021 (155)
139 Qatari NC_000004.11 - 148047550 Apr 26, 2020 (154)
140 SGDP_PRJ NC_000004.11 - 148047550 Apr 26, 2020 (154)
141 Siberian NC_000004.11 - 148047550 Apr 26, 2020 (154)
142 8.3KJPN NC_000004.11 - 148047550 Apr 26, 2021 (155)
143 14KJPN NC_000004.12 - 147126398 Oct 17, 2022 (156)
144 TopMed NC_000004.12 - 147126398 Apr 26, 2021 (155)
145 UK 10K study - Twins NC_000004.11 - 148047550 Oct 12, 2018 (152)
146 A Vietnamese Genetic Variation Database NC_000004.11 - 148047550 Jul 13, 2019 (153)
147 ALFA NC_000004.12 - 147126398 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)
rs17839141 Oct 07, 2004 (123)
rs59818671 May 25, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
13828039, ss3906650645 NC_000004.11:148047549:C:A NC_000004.12:147126397:C:A (self)
13828039, ss3906650645 NC_000004.11:148047549:C:G NC_000004.12:147126397:C:G (self)
ss35361839, ss3639260858, ss3639928668, ss3643974615 NC_000004.9:148405154:C:T NC_000004.12:147126397:C:T (self)
446057, ss92820740, ss108435411, ss110764814, ss162639342, ss164647309, ss167273848, ss199318358, ss206325579, ss253607197, ss277981108, ss285027752, ss293220745, ss1590319502, ss1712714214, ss2635137754, ss3643466382, ss3847768165 NC_000004.10:148266999:C:T NC_000004.12:147126397:C:T (self)
23794738, 13229784, 9396608, 6992185, 5861590, 13828039, 4998079, 327511, 85954, 6090576, 12329822, 3258319, 26522888, 13229784, 2918648, ss221277158, ss232645979, ss239883189, ss491361225, ss536864285, ss557930223, ss651750640, ss780681893, ss783355225, ss832776938, ss980807008, ss1072053247, ss1312301238, ss1430090741, ss1580827246, ss1611425260, ss1654419293, ss1752501949, ss1917785199, ss1924048646, ss1946129408, ss1958728172, ss1969900926, ss2022610304, ss2150741965, ss2625801273, ss2706237426, ss2816657826, ss2985305703, ss2985932767, ss2995752713, ss3022424387, ss3346018164, ss3629088534, ss3629088535, ss3634974609, ss3638517427, ss3640681903, ss3644862246, ss3652914536, ss3654077657, ss3663658360, ss3731713214, ss3744530394, ss3745274828, ss3762558004, ss3772769285, ss3784896029, ss3790327415, ss3795202968, ss3828869931, ss3837885460, ss3860312842, ss3906650645, ss3984536592, ss3985101584, ss4017173820, ss5168553581, ss5314998380, ss5353072012, ss5507776761, ss5624570321, ss5636344511, ss5844880334, ss5848027945, ss5964747664 NC_000004.11:148047549:C:T NC_000004.12:147126397:C:T (self)
31295394, 168536434, 2730743, 381306, 37533474, 473633909, 6938631096, ss2268129014, ss3025082033, ss3647878181, ss3713294722, ss3726179023, ss3771159837, ss3805719662, ss3843325584, ss4636256353, ss5261447503, ss5459956141, ss5543769459, ss5703696370, ss5805643372, ss5854495868, ss5865986539 NC_000004.12:147126397:C:T NC_000004.12:147126397:C:T (self)
ss2191491, ss24153794, ss24782131, ss44521864, ss67094565, ss67429017, ss68153585, ss70613059, ss71160731, ss75764257, ss83753809, ss98872579, ss104127928, ss135100693, ss139947037, ss153412140, ss158036866, ss159264736, ss172469698 NT_016354.19:72595270:C:T NC_000004.12:147126397:C:T (self)
ss17013827, ss22176088 NT_016606.16:9595605:C:T NC_000004.12:147126397: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 rs1395821

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