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dbSNP Short Genetic Variations

Examples: rs268, BRCA1 and more Advanced search

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.

rs27323

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr5:53256409 (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
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.420545 (111314/264690, TOPMED)
G=0.407645 (81507/199946, ALFA)
G=0.418907 (58626/139950, GnomAD) (+ 20 more)
G=0.49232 (13912/28258, 14KJPN)
G=0.49427 (8284/16760, 8.3KJPN)
G=0.4920 (3151/6404, 1000G_30x)
G=0.4982 (2495/5008, 1000G)
G=0.4326 (1938/4480, Estonian)
G=0.3954 (1524/3854, ALSPAC)
G=0.3994 (1481/3708, TWINSUK)
A=0.4997 (1464/2930, KOREAN)
G=0.4933 (1028/2084, HGDP_Stanford)
G=0.4789 (906/1892, HapMap)
A=0.4885 (895/1832, Korea1K)
G=0.365 (364/998, GoNL)
A=0.461 (364/790, PRJEB37584)
G=0.322 (193/600, NorthernSweden)
G=0.314 (130/414, SGDP_PRJ)
G=0.338 (73/216, Qatari)
A=0.315 (68/216, Vietnamese)
G=0.39 (24/62, Ancient Sardinia)
G=0.40 (17/42, Siberian)
G=0.33 (13/40, 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 199946 G=0.407645 A=0.592355
European Sub 172756 G=0.401630 A=0.598370
African Sub 7094 G=0.4412 A=0.5588
African Others Sub 264 G=0.492 A=0.508
African American Sub 6830 G=0.4392 A=0.5608
Asian Sub 702 G=0.564 A=0.436
East Asian Sub 556 G=0.570 A=0.430
Other Asian Sub 146 G=0.541 A=0.459
Latin American 1 Sub 844 G=0.358 A=0.642
Latin American 2 Sub 6908 G=0.3919 A=0.6081
South Asian Sub 5042 G=0.5635 A=0.4365
Other Sub 6600 G=0.4162 A=0.5838


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=0.420545 A=0.579455
Allele Frequency Aggregator Total Global 199946 G=0.407645 A=0.592355
Allele Frequency Aggregator European Sub 172756 G=0.401630 A=0.598370
Allele Frequency Aggregator African Sub 7094 G=0.4412 A=0.5588
Allele Frequency Aggregator Latin American 2 Sub 6908 G=0.3919 A=0.6081
Allele Frequency Aggregator Other Sub 6600 G=0.4162 A=0.5838
Allele Frequency Aggregator South Asian Sub 5042 G=0.5635 A=0.4365
Allele Frequency Aggregator Latin American 1 Sub 844 G=0.358 A=0.642
Allele Frequency Aggregator Asian Sub 702 G=0.564 A=0.436
gnomAD - Genomes Global Study-wide 139950 G=0.418907 A=0.581093
gnomAD - Genomes European Sub 75830 G=0.39856 A=0.60144
gnomAD - Genomes African Sub 41926 G=0.44011 A=0.55989
gnomAD - Genomes American Sub 13614 G=0.42449 A=0.57551
gnomAD - Genomes Ashkenazi Jewish Sub 3322 G=0.4548 A=0.5452
gnomAD - Genomes East Asian Sub 3110 G=0.5749 A=0.4251
gnomAD - Genomes Other Sub 2148 G=0.4064 A=0.5936
14KJPN JAPANESE Study-wide 28258 G=0.49232 A=0.50768
8.3KJPN JAPANESE Study-wide 16760 G=0.49427 A=0.50573
1000Genomes_30x Global Study-wide 6404 G=0.4920 A=0.5080
1000Genomes_30x African Sub 1786 G=0.4513 A=0.5487
1000Genomes_30x Europe Sub 1266 G=0.3926 A=0.6074
1000Genomes_30x South Asian Sub 1202 G=0.5990 A=0.4010
1000Genomes_30x East Asian Sub 1170 G=0.5949 A=0.4051
1000Genomes_30x American Sub 980 G=0.441 A=0.559
1000Genomes Global Study-wide 5008 G=0.4982 A=0.5018
1000Genomes African Sub 1322 G=0.4546 A=0.5454
1000Genomes East Asian Sub 1008 G=0.6002 A=0.3998
1000Genomes Europe Sub 1006 G=0.3936 A=0.6064
1000Genomes South Asian Sub 978 G=0.597 A=0.403
1000Genomes American Sub 694 G=0.445 A=0.555
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.4326 A=0.5674
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.3954 A=0.6046
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.3994 A=0.6006
KOREAN population from KRGDB KOREAN Study-wide 2930 G=0.5003 A=0.4997
HGDP-CEPH-db Supplement 1 Global Study-wide 2084 G=0.4933 A=0.5067
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 G=0.589 A=0.411
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 G=0.486 A=0.514
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 G=0.420 A=0.580
HGDP-CEPH-db Supplement 1 Europe Sub 320 G=0.441 A=0.559
HGDP-CEPH-db Supplement 1 Africa Sub 242 G=0.496 A=0.504
HGDP-CEPH-db Supplement 1 America Sub 216 G=0.528 A=0.472
HGDP-CEPH-db Supplement 1 Oceania Sub 72 G=0.39 A=0.61
HapMap Global Study-wide 1892 G=0.4789 A=0.5211
HapMap American Sub 770 G=0.468 A=0.532
HapMap African Sub 692 G=0.514 A=0.486
HapMap Asian Sub 254 G=0.492 A=0.508
HapMap Europe Sub 176 G=0.369 A=0.631
Korean Genome Project KOREAN Study-wide 1832 G=0.5115 A=0.4885
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.365 A=0.635
CNV burdens in cranial meningiomas Global Study-wide 790 G=0.539 A=0.461
CNV burdens in cranial meningiomas CRM Sub 790 G=0.539 A=0.461
Northern Sweden ACPOP Study-wide 600 G=0.322 A=0.678
SGDP_PRJ Global Study-wide 414 G=0.314 A=0.686
Qatari Global Study-wide 216 G=0.338 A=0.662
A Vietnamese Genetic Variation Database Global Study-wide 216 G=0.685 A=0.315
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 62 G=0.39 A=0.61
Siberian Global Study-wide 42 G=0.40 A=0.60
The Danish reference pan genome Danish Study-wide 40 G=0.33 A=0.68
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.53256409G>A
GRCh37.p13 chr 5 NC_000005.9:g.52552239G>A
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
GRCh38.p14 chr 5 NC_000005.10:g.53256409= NC_000005.10:g.53256409G>A
GRCh37.p13 chr 5 NC_000005.9:g.52552239= NC_000005.9:g.52552239G>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#.

135 SubSNP, 23 Frequency submissions
No Submitter Submission ID Date (Build)
1 KWOK ss42211 May 08, 2000 (76)
2 KWOK ss42626 May 08, 2000 (76)
3 SC_JCM ss571870 Jul 16, 2000 (80)
4 KWOK ss892732 Oct 04, 2000 (86)
5 KWOK ss1003271 Oct 04, 2000 (86)
6 KWOK ss1994555 Oct 18, 2000 (87)
7 KWOK ss2044210 Oct 18, 2000 (87)
8 TSC-CSHL ss2260079 Oct 23, 2000 (88)
9 SSAHASNP ss22293574 Apr 05, 2004 (121)
10 PERLEGEN ss23918388 Sep 20, 2004 (123)
11 ABI ss44611987 Mar 15, 2006 (126)
12 ILLUMINA ss66777254 Nov 30, 2006 (127)
13 ILLUMINA ss67270594 Nov 30, 2006 (127)
14 ILLUMINA ss67671167 Nov 30, 2006 (127)
15 ILLUMINA ss70749044 May 24, 2008 (130)
16 ILLUMINA ss71321177 May 17, 2007 (127)
17 ILLUMINA ss75769668 Dec 07, 2007 (129)
18 HGSV ss78360168 Dec 07, 2007 (129)
19 HGSV ss78976628 Dec 07, 2007 (129)
20 ILLUMINA ss79145258 Dec 15, 2007 (130)
21 KRIBB_YJKIM ss83353314 Dec 15, 2007 (130)
22 HUMANGENOME_JCVI ss98617696 Feb 04, 2009 (130)
23 1000GENOMES ss109028611 Jan 23, 2009 (130)
24 1000GENOMES ss111820309 Jan 25, 2009 (130)
25 ILLUMINA-UK ss116607805 Feb 14, 2009 (130)
26 ILLUMINA ss122095326 Dec 01, 2009 (131)
27 ENSEMBL ss144211894 Dec 01, 2009 (131)
28 ILLUMINA ss154231204 Dec 01, 2009 (131)
29 GMI ss155419411 Dec 01, 2009 (131)
30 ILLUMINA ss159407709 Dec 01, 2009 (131)
31 ILLUMINA ss160574387 Dec 01, 2009 (131)
32 COMPLETE_GENOMICS ss162241013 Jul 04, 2010 (132)
33 COMPLETE_GENOMICS ss164911096 Jul 04, 2010 (132)
34 COMPLETE_GENOMICS ss166524790 Jul 04, 2010 (132)
35 ILLUMINA ss171360866 Jul 04, 2010 (132)
36 ILLUMINA ss173446747 Jul 04, 2010 (132)
37 BUSHMAN ss200236004 Jul 04, 2010 (132)
38 1000GENOMES ss221672898 Jul 14, 2010 (132)
39 1000GENOMES ss232940915 Jul 14, 2010 (132)
40 1000GENOMES ss240115017 Jul 15, 2010 (132)
41 BL ss253450519 May 09, 2011 (134)
42 GMI ss278287114 May 04, 2012 (137)
43 GMI ss285174896 Apr 25, 2013 (138)
44 PJP ss293355171 May 09, 2011 (134)
45 ILLUMINA ss480649603 May 04, 2012 (137)
46 ILLUMINA ss480664970 May 04, 2012 (137)
47 ILLUMINA ss481511682 Sep 08, 2015 (146)
48 ILLUMINA ss485119733 May 04, 2012 (137)
49 ILLUMINA ss537121486 Sep 08, 2015 (146)
50 TISHKOFF ss558383561 Apr 25, 2013 (138)
51 SSMP ss652250130 Apr 25, 2013 (138)
52 ILLUMINA ss778877573 Sep 08, 2015 (146)
53 ILLUMINA ss783006210 Sep 08, 2015 (146)
54 ILLUMINA ss783966584 Sep 08, 2015 (146)
55 ILLUMINA ss825475776 Jul 19, 2016 (147)
56 ILLUMINA ss832263466 Sep 08, 2015 (146)
57 ILLUMINA ss832919400 Jul 13, 2019 (153)
58 ILLUMINA ss834338541 Sep 08, 2015 (146)
59 EVA-GONL ss981551442 Aug 21, 2014 (142)
60 JMKIDD_LAB ss1072620660 Aug 21, 2014 (142)
61 1000GENOMES ss1315054259 Aug 21, 2014 (142)
62 DDI ss1430338644 Apr 01, 2015 (144)
63 EVA_GENOME_DK ss1581132067 Apr 01, 2015 (144)
64 EVA_DECODE ss1591069926 Apr 01, 2015 (144)
65 EVA_UK10K_ALSPAC ss1612864944 Apr 01, 2015 (144)
66 EVA_UK10K_TWINSUK ss1655858977 Apr 01, 2015 (144)
67 EVA_SVP ss1712762851 Apr 01, 2015 (144)
68 ILLUMINA ss1752577550 Sep 08, 2015 (146)
69 HAMMER_LAB ss1803499656 Sep 08, 2015 (146)
70 WEILL_CORNELL_DGM ss1924811507 Feb 12, 2016 (147)
71 GENOMED ss1970084399 Jul 19, 2016 (147)
72 JJLAB ss2023008398 Sep 14, 2016 (149)
73 USC_VALOUEV ss2151163789 Dec 20, 2016 (150)
74 HUMAN_LONGEVITY ss2273600058 Dec 20, 2016 (150)
75 SYSTEMSBIOZJU ss2626001161 Nov 08, 2017 (151)
76 ILLUMINA ss2634277372 Nov 08, 2017 (151)
77 GRF ss2706705767 Nov 08, 2017 (151)
78 GNOMAD ss2824473213 Nov 08, 2017 (151)
79 SWEGEN ss2996913550 Nov 08, 2017 (151)
80 ILLUMINA ss3022487588 Nov 08, 2017 (151)
81 BIOINF_KMB_FNS_UNIBA ss3025287917 Nov 08, 2017 (151)
82 CSHL ss3346381461 Nov 08, 2017 (151)
83 ILLUMINA ss3629232421 Oct 12, 2018 (152)
84 ILLUMINA ss3632204602 Oct 12, 2018 (152)
85 ILLUMINA ss3633373627 Oct 12, 2018 (152)
86 ILLUMINA ss3634094182 Oct 12, 2018 (152)
87 ILLUMINA ss3635001160 Oct 12, 2018 (152)
88 ILLUMINA ss3635776229 Oct 12, 2018 (152)
89 ILLUMINA ss3636711980 Oct 12, 2018 (152)
90 ILLUMINA ss3637528832 Oct 12, 2018 (152)
91 ILLUMINA ss3638552767 Oct 12, 2018 (152)
92 ILLUMINA ss3639278901 Oct 12, 2018 (152)
93 ILLUMINA ss3639662610 Oct 12, 2018 (152)
94 ILLUMINA ss3640708453 Oct 12, 2018 (152)
95 ILLUMINA ss3643498713 Oct 12, 2018 (152)
96 URBANLAB ss3648057532 Oct 12, 2018 (152)
97 ILLUMINA ss3652983266 Oct 12, 2018 (152)
98 EGCUT_WGS ss3664790892 Jul 13, 2019 (153)
99 EVA_DECODE ss3714662904 Jul 13, 2019 (153)
100 ILLUMINA ss3726231882 Jul 13, 2019 (153)
101 ACPOP ss3732344240 Jul 13, 2019 (153)
102 ILLUMINA ss3745301376 Jul 13, 2019 (153)
103 EVA ss3763417094 Jul 13, 2019 (153)
104 ILLUMINA ss3772795588 Jul 13, 2019 (153)
105 PACBIO ss3785106301 Jul 13, 2019 (153)
106 PACBIO ss3790513499 Jul 13, 2019 (153)
107 PACBIO ss3795390110 Jul 13, 2019 (153)
108 KHV_HUMAN_GENOMES ss3806589733 Jul 13, 2019 (153)
109 EVA ss3829236854 Apr 26, 2020 (154)
110 EVA ss3838089594 Apr 26, 2020 (154)
111 EVA ss3843530053 Apr 26, 2020 (154)
112 HGDP ss3847789960 Apr 26, 2020 (154)
113 SGDP_PRJ ss3861831066 Apr 26, 2020 (154)
114 KRGDB ss3908362374 Apr 26, 2020 (154)
115 KOGIC ss3956667436 Apr 26, 2020 (154)
116 EVA ss3984546772 Apr 26, 2021 (155)
117 EVA ss3985139835 Apr 26, 2021 (155)
118 EVA ss4017206031 Apr 26, 2021 (155)
119 TOPMED ss4659546704 Apr 26, 2021 (155)
120 TOMMO_GENOMICS ss5171690251 Apr 26, 2021 (155)
121 1000G_HIGH_COVERAGE ss5263933803 Oct 13, 2022 (156)
122 EVA ss5315050423 Oct 13, 2022 (156)
123 EVA ss5357496195 Oct 13, 2022 (156)
124 HUGCELL_USP ss5462121588 Oct 13, 2022 (156)
125 EVA ss5508017452 Oct 13, 2022 (156)
126 1000G_HIGH_COVERAGE ss5547564779 Oct 13, 2022 (156)
127 SANFORD_IMAGENETICS ss5624588725 Oct 13, 2022 (156)
128 SANFORD_IMAGENETICS ss5637780539 Oct 13, 2022 (156)
129 TOMMO_GENOMICS ss5708071871 Oct 13, 2022 (156)
130 EVA ss5799648091 Oct 13, 2022 (156)
131 YY_MCH ss5806312926 Oct 13, 2022 (156)
132 EVA ss5834911612 Oct 13, 2022 (156)
133 EVA ss5854808002 Oct 13, 2022 (156)
134 EVA ss5894139323 Oct 13, 2022 (156)
135 EVA ss5966202911 Oct 13, 2022 (156)
136 1000Genomes NC_000005.9 - 52552239 Oct 12, 2018 (152)
137 1000Genomes_30x NC_000005.10 - 53256409 Oct 13, 2022 (156)
138 The Avon Longitudinal Study of Parents and Children NC_000005.9 - 52552239 Oct 12, 2018 (152)
139 Genetic variation in the Estonian population NC_000005.9 - 52552239 Oct 12, 2018 (152)
140 The Danish reference pan genome NC_000005.9 - 52552239 Apr 26, 2020 (154)
141 gnomAD - Genomes NC_000005.10 - 53256409 Apr 26, 2021 (155)
142 Genome of the Netherlands Release 5 NC_000005.9 - 52552239 Apr 26, 2020 (154)
143 HGDP-CEPH-db Supplement 1 NC_000005.8 - 52587996 Apr 26, 2020 (154)
144 HapMap NC_000005.10 - 53256409 Apr 26, 2020 (154)
145 KOREAN population from KRGDB NC_000005.9 - 52552239 Apr 26, 2020 (154)
146 Korean Genome Project NC_000005.10 - 53256409 Apr 26, 2020 (154)
147 Northern Sweden NC_000005.9 - 52552239 Jul 13, 2019 (153)
148 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000005.9 - 52552239 Apr 26, 2021 (155)
149 CNV burdens in cranial meningiomas NC_000005.9 - 52552239 Apr 26, 2021 (155)
150 Qatari NC_000005.9 - 52552239 Apr 26, 2020 (154)
151 SGDP_PRJ NC_000005.9 - 52552239 Apr 26, 2020 (154)
152 Siberian NC_000005.9 - 52552239 Apr 26, 2020 (154)
153 8.3KJPN NC_000005.9 - 52552239 Apr 26, 2021 (155)
154 14KJPN NC_000005.10 - 53256409 Oct 13, 2022 (156)
155 TopMed NC_000005.10 - 53256409 Apr 26, 2021 (155)
156 UK 10K study - Twins NC_000005.9 - 52552239 Oct 12, 2018 (152)
157 A Vietnamese Genetic Variation Database NC_000005.9 - 52552239 Jul 13, 2019 (153)
158 ALFA NC_000005.10 - 53256409 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)
rs58373636 May 24, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
467852, ss78360168, ss78976628, ss109028611, ss111820309, ss116607805, ss162241013, ss164911096, ss166524790, ss200236004, ss253450519, ss278287114, ss285174896, ss293355171, ss480649603, ss825475776, ss1591069926, ss1712762851, ss3639278901, ss3639662610, ss3643498713, ss3847789960 NC_000005.8:52587995:G:A NC_000005.10:53256408:G:A (self)
26651812, 14813958, 10529140, 7297006, 6584872, 15539768, 5629105, 365762, 96138, 6853437, 13848046, 3680143, 29659558, 14813958, 3291294, ss221672898, ss232940915, ss240115017, ss480664970, ss481511682, ss485119733, ss537121486, ss558383561, ss652250130, ss778877573, ss783006210, ss783966584, ss832263466, ss832919400, ss834338541, ss981551442, ss1072620660, ss1315054259, ss1430338644, ss1581132067, ss1612864944, ss1655858977, ss1752577550, ss1803499656, ss1924811507, ss1970084399, ss2023008398, ss2151163789, ss2626001161, ss2634277372, ss2706705767, ss2824473213, ss2996913550, ss3022487588, ss3346381461, ss3629232421, ss3632204602, ss3633373627, ss3634094182, ss3635001160, ss3635776229, ss3636711980, ss3637528832, ss3638552767, ss3640708453, ss3652983266, ss3664790892, ss3732344240, ss3745301376, ss3763417094, ss3772795588, ss3785106301, ss3790513499, ss3795390110, ss3829236854, ss3838089594, ss3861831066, ss3908362374, ss3984546772, ss3985139835, ss4017206031, ss5171690251, ss5315050423, ss5357496195, ss5508017452, ss5624588725, ss5637780539, ss5799648091, ss5834911612, ss5966202911 NC_000005.9:52552238:G:A NC_000005.10:53256408:G:A (self)
35090714, 188331551, 2863648, 13045437, 41908975, 496924261, 11521085735, ss2273600058, ss3025287917, ss3648057532, ss3714662904, ss3726231882, ss3806589733, ss3843530053, ss3956667436, ss4659546704, ss5263933803, ss5462121588, ss5547564779, ss5708071871, ss5806312926, ss5854808002, ss5894139323 NC_000005.10:53256408:G:A NC_000005.10:53256408:G:A (self)
ss22293574 NT_006431.13:3116981:G:A NC_000005.10:53256408:G:A (self)
ss42211, ss42626, ss571870, ss892732, ss1003271, ss1994555, ss2044210, ss2260079, ss23918388, ss44611987, ss66777254, ss67270594, ss67671167, ss70749044, ss71321177, ss75769668, ss79145258, ss83353314, ss98617696, ss122095326, ss144211894, ss154231204, ss155419411, ss159407709, ss160574387, ss171360866, ss173446747 NT_006713.15:3146597:G:A NC_000005.10:53256408:G:A (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 rs27323

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