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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.

rs2411453

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr16:28620700 (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
T>C / T>G
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.487891 (129140/264690, TOPMED)
G=0.484257 (67796/140000, GnomAD)
T=0.43848 (22111/50426, ALFA) (+ 16 more)
T=0.23756 (6713/28258, 14KJPN)
T=0.23872 (4001/16760, 8.3KJPN)
T=0.4825 (3090/6404, 1000G_30x)
T=0.4655 (2331/5008, 1000G)
T=0.3978 (1533/3854, ALSPAC)
T=0.4129 (1531/3708, TWINSUK)
T=0.2273 (666/2930, KOREAN)
T=0.2282 (418/1832, Korea1K)
T=0.4947 (744/1504, HapMap)
T=0.382 (381/998, GoNL)
T=0.420 (252/600, NorthernSweden)
T=0.239 (91/380, SGDP_PRJ)
T=0.273 (59/216, Qatari)
T=0.286 (60/210, Vietnamese)
T=0.31 (15/48, Siberian)
G=0.47 (19/40, GENOME_DK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
SULT1A1 : 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 55456 T=0.44350 G=0.55650
European Sub 44518 T=0.40514 G=0.59486
African Sub 5240 T=0.7595 G=0.2405
African Others Sub 182 T=0.852 G=0.148
African American Sub 5058 T=0.7562 G=0.2438
Asian Sub 238 T=0.311 G=0.689
East Asian Sub 180 T=0.278 G=0.722
Other Asian Sub 58 T=0.41 G=0.59
Latin American 1 Sub 250 T=0.508 G=0.492
Latin American 2 Sub 1920 T=0.4938 G=0.5062
South Asian Sub 116 T=0.216 G=0.784
Other Sub 3174 T=0.4427 G=0.5573


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 T=0.512109 G=0.487891
gnomAD - Genomes Global Study-wide 140000 T=0.515743 G=0.484257
gnomAD - Genomes European Sub 75810 T=0.41418 G=0.58582
gnomAD - Genomes African Sub 41956 T=0.74650 G=0.25350
gnomAD - Genomes American Sub 13636 T=0.47096 G=0.52904
gnomAD - Genomes Ashkenazi Jewish Sub 3322 T=0.3555 G=0.6445
gnomAD - Genomes East Asian Sub 3126 T=0.2908 G=0.7092
gnomAD - Genomes Other Sub 2150 T=0.4526 G=0.5474
Allele Frequency Aggregator Total Global 50426 T=0.43848 G=0.56152
Allele Frequency Aggregator European Sub 41428 T=0.40521 G=0.59479
Allele Frequency Aggregator African Sub 4098 T=0.7592 G=0.2408
Allele Frequency Aggregator Other Sub 2376 T=0.4373 G=0.5627
Allele Frequency Aggregator Latin American 2 Sub 1920 T=0.4938 G=0.5062
Allele Frequency Aggregator Latin American 1 Sub 250 T=0.508 G=0.492
Allele Frequency Aggregator Asian Sub 238 T=0.311 G=0.689
Allele Frequency Aggregator South Asian Sub 116 T=0.216 G=0.784
14KJPN JAPANESE Study-wide 28258 T=0.23756 G=0.76244
8.3KJPN JAPANESE Study-wide 16760 T=0.23872 G=0.76128
1000Genomes_30x Global Study-wide 6404 T=0.4825 G=0.5175
1000Genomes_30x African Sub 1786 T=0.8046 G=0.1954
1000Genomes_30x Europe Sub 1266 T=0.3539 G=0.6461
1000Genomes_30x South Asian Sub 1202 T=0.2554 G=0.7446
1000Genomes_30x East Asian Sub 1170 T=0.3137 G=0.6863
1000Genomes_30x American Sub 980 T=0.542 G=0.458
1000Genomes Global Study-wide 5008 T=0.4655 G=0.5345
1000Genomes African Sub 1322 T=0.7897 G=0.2103
1000Genomes East Asian Sub 1008 T=0.3046 G=0.6954
1000Genomes Europe Sub 1006 T=0.3529 G=0.6471
1000Genomes South Asian Sub 978 T=0.257 G=0.743
1000Genomes American Sub 694 T=0.539 G=0.461
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 T=0.3978 G=0.6022
UK 10K study - Twins TWIN COHORT Study-wide 3708 T=0.4129 G=0.5871
KOREAN population from KRGDB KOREAN Study-wide 2930 T=0.2273 C=0.0000, G=0.7727
Korean Genome Project KOREAN Study-wide 1832 T=0.2282 G=0.7718
HapMap Global Study-wide 1504 T=0.4947 G=0.5053
HapMap African Sub 684 T=0.716 G=0.284
HapMap American Sub 394 T=0.358 G=0.642
HapMap Asian Sub 250 T=0.228 G=0.772
HapMap Europe Sub 176 T=0.318 G=0.682
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 T=0.382 G=0.618
Northern Sweden ACPOP Study-wide 600 T=0.420 G=0.580
SGDP_PRJ Global Study-wide 380 T=0.239 G=0.761
Qatari Global Study-wide 216 T=0.273 G=0.727
A Vietnamese Genetic Variation Database Global Study-wide 210 T=0.286 G=0.714
Siberian Global Study-wide 48 T=0.31 G=0.69
The Danish reference pan genome Danish Study-wide 40 T=0.53 G=0.47
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 16 NC_000016.10:g.28620700T>C
GRCh38.p14 chr 16 NC_000016.10:g.28620700T>G
GRCh37.p13 chr 16 NC_000016.9:g.28632021T>C
GRCh37.p13 chr 16 NC_000016.9:g.28632021T>G
SULT1A1 RefSeqGene NG_028128.1:g.7846A>G
SULT1A1 RefSeqGene NG_028128.1:g.7846A>C
Gene: SULT1A1, sulfotransferase family 1A member 1 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
SULT1A1 transcript variant 6 NM_001394421.1:c.-409-567…

NM_001394421.1:c.-409-567A>G

 		N/A Intron Variant
SULT1A1 transcript variant 7 NM_001394422.1:c.-1208-56…

NM_001394422.1:c.-1208-567A>G

 		N/A Intron Variant
SULT1A1 transcript variant 8 NM_001394423.1:c.-539-567…

NM_001394423.1:c.-539-567A>G

 		N/A Intron Variant
SULT1A1 transcript variant 9 NM_001394424.1:c.-106-567…

NM_001394424.1:c.-106-567A>G

 		N/A Intron Variant
SULT1A1 transcript variant 10 NM_001394425.1:c.-336-567…

NM_001394425.1:c.-336-567A>G

 		N/A Intron Variant
SULT1A1 transcript variant 5 NM_177536.5:c.-2-567A>G N/A Intron Variant
SULT1A1 transcript variant 1 NM_001055.4:c. N/A Genic Upstream Transcript Variant
SULT1A1 transcript variant 2 NM_177529.3:c. N/A Genic Upstream Transcript Variant
SULT1A1 transcript variant 3 NM_177530.4:c. N/A Genic Upstream Transcript Variant
SULT1A1 transcript variant 4 NM_177534.4:c. N/A Genic Upstream Transcript Variant
SULT1A1 transcript variant X8 XM_047434547.1:c.-75-567A…

XM_047434547.1:c.-75-567A>G

 		N/A Intron Variant
SULT1A1 transcript variant X10 XM_047434549.1:c.68-567A>G N/A Intron Variant
SULT1A1 transcript variant X2 XM_017023604.2:c. N/A Genic Upstream Transcript Variant
SULT1A1 transcript variant X7 XM_017023605.2:c. N/A Genic Upstream Transcript Variant
SULT1A1 transcript variant X1 XM_017023608.2:c. N/A Genic Upstream Transcript Variant
SULT1A1 transcript variant X4 XM_017023610.2:c. N/A Genic Upstream Transcript Variant
SULT1A1 transcript variant X3 XM_047434544.1:c. N/A Genic Upstream Transcript Variant
SULT1A1 transcript variant X5 XM_047434545.1:c. N/A Genic Upstream Transcript Variant
SULT1A1 transcript variant X6 XM_047434546.1:c. N/A Genic Upstream Transcript Variant
SULT1A1 transcript variant X9 XM_047434548.1:c. N/A Genic Upstream Transcript Variant
SULT1A1 transcript variant X11 XM_047434550.1: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 T= C G
GRCh38.p14 chr 16 NC_000016.10:g.28620700= NC_000016.10:g.28620700T>C NC_000016.10:g.28620700T>G
GRCh37.p13 chr 16 NC_000016.9:g.28632021= NC_000016.9:g.28632021T>C NC_000016.9:g.28632021T>G
SULT1A1 RefSeqGene NG_028128.1:g.7846= NG_028128.1:g.7846A>G NG_028128.1:g.7846A>C
SULT1A1 transcript variant 6 NM_001394421.1:c.-409-567= NM_001394421.1:c.-409-567A>G NM_001394421.1:c.-409-567A>C
SULT1A1 transcript variant 7 NM_001394422.1:c.-1208-567= NM_001394422.1:c.-1208-567A>G NM_001394422.1:c.-1208-567A>C
SULT1A1 transcript variant 8 NM_001394423.1:c.-539-567= NM_001394423.1:c.-539-567A>G NM_001394423.1:c.-539-567A>C
SULT1A1 transcript variant 9 NM_001394424.1:c.-106-567= NM_001394424.1:c.-106-567A>G NM_001394424.1:c.-106-567A>C
SULT1A1 transcript variant 10 NM_001394425.1:c.-336-567= NM_001394425.1:c.-336-567A>G NM_001394425.1:c.-336-567A>C
SULT1A1 transcript variant 5 NM_177536.3:c.68-567= NM_177536.3:c.68-567A>G NM_177536.3:c.68-567A>C
SULT1A1 transcript variant 5 NM_177536.5:c.-2-567= NM_177536.5:c.-2-567A>G NM_177536.5:c.-2-567A>C
SULT1A1 transcript variant X1 XM_005255522.1:c.-336-567= XM_005255522.1:c.-336-567A>G XM_005255522.1:c.-336-567A>C
SULT1A1 transcript variant X8 XM_047434547.1:c.-75-567= XM_047434547.1:c.-75-567A>G XM_047434547.1:c.-75-567A>C
SULT1A1 transcript variant X10 XM_047434549.1:c.68-567= XM_047434549.1:c.68-567A>G XM_047434549.1:c.68-567A>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, 19 Frequency submissions
No Submitter Submission ID Date (Build)
1 TSC-CSHL ss3378064 Sep 28, 2001 (100)
2 BCM_SSAHASNP ss10816671 Jul 11, 2003 (116)
3 WI_SSAHASNP ss12357592 Jul 11, 2003 (116)
4 PERLEGEN ss24454391 Sep 20, 2004 (123)
5 PERLEGEN ss69342944 May 17, 2007 (127)
6 AFFY ss76787004 Dec 06, 2007 (129)
7 HGSV ss83075069 Dec 16, 2007 (130)
8 HGSV ss83374042 Dec 16, 2007 (130)
9 HGSV ss83820108 Dec 16, 2007 (130)
10 HUMANGENOME_JCVI ss96633271 Feb 06, 2009 (130)
11 KRIBB_YJKIM ss104871679 Feb 06, 2009 (130)
12 1000GENOMES ss109294000 Jan 23, 2009 (130)
13 1000GENOMES ss115017968 Jan 25, 2009 (130)
14 ENSEMBL ss136654067 Dec 01, 2009 (131)
15 ENSEMBL ss136762993 Dec 01, 2009 (131)
16 GMI ss157237952 Dec 01, 2009 (131)
17 COMPLETE_GENOMICS ss168101511 Jul 04, 2010 (132)
18 COMPLETE_GENOMICS ss169552561 Jul 04, 2010 (132)
19 BCM-HGSC-SUB ss207484781 Jul 04, 2010 (132)
20 1000GENOMES ss237002525 Jul 15, 2010 (132)
21 1000GENOMES ss243346966 Jul 15, 2010 (132)
22 GMI ss282489836 May 04, 2012 (137)
23 GMI ss287057503 Apr 25, 2013 (138)
24 PJP ss291943367 May 09, 2011 (134)
25 ILLUMINA ss410816022 Sep 17, 2011 (135)
26 ILLUMINA ss535738625 Sep 08, 2015 (146)
27 TISHKOFF ss564864814 Apr 25, 2013 (138)
28 SSMP ss660617013 Apr 25, 2013 (138)
29 EVA-GONL ss992420768 Aug 21, 2014 (142)
30 JMKIDD_LAB ss1080583601 Aug 21, 2014 (142)
31 1000GENOMES ss1355922896 Aug 21, 2014 (142)
32 DDI ss1427820631 Apr 01, 2015 (144)
33 EVA_GENOME_DK ss1577891425 Apr 01, 2015 (144)
34 EVA_UK10K_ALSPAC ss1634284218 Apr 01, 2015 (144)
35 EVA_UK10K_TWINSUK ss1677278251 Apr 01, 2015 (144)
36 EVA_DECODE ss1696455412 Apr 01, 2015 (144)
37 EVA_SVP ss1713535416 Apr 01, 2015 (144)
38 HAMMER_LAB ss1808484475 Sep 08, 2015 (146)
39 WEILL_CORNELL_DGM ss1935844667 Feb 12, 2016 (147)
40 ILLUMINA ss1946412992 Feb 12, 2016 (147)
41 ILLUMINA ss1959671770 Feb 12, 2016 (147)
42 GENOMED ss1968249529 Jul 19, 2016 (147)
43 JJLAB ss2028710617 Sep 14, 2016 (149)
44 USC_VALOUEV ss2157123360 Dec 20, 2016 (150)
45 SYSTEMSBIOZJU ss2628848060 Nov 08, 2017 (151)
46 GRF ss2701629484 Nov 08, 2017 (151)
47 ILLUMINA ss2710831001 Nov 08, 2017 (151)
48 GNOMAD ss2941921924 Nov 08, 2017 (151)
49 SWEGEN ss3014307408 Nov 08, 2017 (151)
50 ILLUMINA ss3021697993 Nov 08, 2017 (151)
51 BIOINF_KMB_FNS_UNIBA ss3028179016 Nov 08, 2017 (151)
52 CSHL ss3351403109 Nov 08, 2017 (151)
53 ILLUMINA ss3627508429 Oct 12, 2018 (152)
54 ILLUMINA ss3644666061 Oct 12, 2018 (152)
55 URBANLAB ss3650495918 Oct 12, 2018 (152)
56 ILLUMINA ss3652104956 Oct 12, 2018 (152)
57 EVA_DECODE ss3699111206 Jul 13, 2019 (153)
58 ILLUMINA ss3725555978 Jul 13, 2019 (153)
59 ACPOP ss3741455413 Jul 13, 2019 (153)
60 ILLUMINA ss3744140358 Jul 13, 2019 (153)
61 EVA ss3753849011 Jul 13, 2019 (153)
62 PACBIO ss3788019003 Jul 13, 2019 (153)
63 PACBIO ss3793006261 Jul 13, 2019 (153)
64 PACBIO ss3797891188 Jul 13, 2019 (153)
65 KHV_HUMAN_GENOMES ss3819142935 Jul 13, 2019 (153)
66 EVA ss3834542067 Apr 27, 2020 (154)
67 EVA ss3840878060 Apr 27, 2020 (154)
68 EVA ss3846369101 Apr 27, 2020 (154)
69 SGDP_PRJ ss3884253521 Apr 27, 2020 (154)
70 KRGDB ss3933595618 Apr 27, 2020 (154)
71 KOGIC ss3977371808 Apr 27, 2020 (154)
72 TOPMED ss5012333819 Apr 27, 2021 (155)
73 TOMMO_GENOMICS ss5219105243 Apr 27, 2021 (155)
74 1000G_HIGH_COVERAGE ss5300634234 Oct 17, 2022 (156)
75 HUGCELL_USP ss5494076552 Oct 17, 2022 (156)
76 1000G_HIGH_COVERAGE ss5603096389 Oct 17, 2022 (156)
77 SANFORD_IMAGENETICS ss5658741773 Oct 17, 2022 (156)
78 TOMMO_GENOMICS ss5773783912 Oct 17, 2022 (156)
79 YY_MCH ss5815881407 Oct 17, 2022 (156)
80 EVA ss5846295563 Oct 17, 2022 (156)
81 EVA ss5851546025 Oct 17, 2022 (156)
82 EVA ss5898802591 Oct 17, 2022 (156)
83 EVA ss5950162329 Oct 17, 2022 (156)
84 1000Genomes NC_000016.9 - 28632021 Oct 12, 2018 (152)
85 1000Genomes_30x NC_000016.10 - 28620700 Oct 17, 2022 (156)
86 The Avon Longitudinal Study of Parents and Children NC_000016.9 - 28632021 Oct 12, 2018 (152)
87 The Danish reference pan genome NC_000016.9 - 28632021 Apr 27, 2020 (154)
88 gnomAD - Genomes NC_000016.10 - 28620700 Apr 27, 2021 (155)
89 Genome of the Netherlands Release 5 NC_000016.9 - 28632021 Apr 27, 2020 (154)
90 HapMap NC_000016.10 - 28620700 Apr 27, 2020 (154)
91 KOREAN population from KRGDB NC_000016.9 - 28632021 Apr 27, 2020 (154)
92 Korean Genome Project NC_000016.10 - 28620700 Apr 27, 2020 (154)
93 Northern Sweden NC_000016.9 - 28632021 Jul 13, 2019 (153)
94 Qatari NC_000016.9 - 28632021 Apr 27, 2020 (154)
95 SGDP_PRJ NC_000016.9 - 28632021 Apr 27, 2020 (154)
96 Siberian NC_000016.9 - 28632021 Apr 27, 2020 (154)
97 8.3KJPN NC_000016.9 - 28632021 Apr 27, 2021 (155)
98 14KJPN NC_000016.10 - 28620700 Oct 17, 2022 (156)
99 TopMed NC_000016.10 - 28620700 Apr 27, 2021 (155)
100 UK 10K study - Twins NC_000016.9 - 28632021 Oct 12, 2018 (152)
101 A Vietnamese Genetic Variation Database NC_000016.9 - 28632021 Jul 13, 2019 (153)
102 ALFA NC_000016.10 - 28620700 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)
rs17526274 Oct 08, 2004 (123)
rs61230324 May 26, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
40773012, ss3933595618 NC_000016.9:28632020:T:C NC_000016.10:28620699:T:C (self)
ss83075069, ss83374042, ss83820108, ss109294000, ss115017968, ss168101511, ss169552561, ss207484781, ss282489836, ss287057503, ss291943367, ss1696455412, ss1713535416 NC_000016.8:28539521:T:G NC_000016.10:28620699:T:G (self)
69075948, 38346944, 4104798, 17104443, 40773012, 14740278, 17886589, 36270501, 9639714, 77074550, 38346944, 8514964, ss237002525, ss243346966, ss535738625, ss564864814, ss660617013, ss992420768, ss1080583601, ss1355922896, ss1427820631, ss1577891425, ss1634284218, ss1677278251, ss1808484475, ss1935844667, ss1946412992, ss1959671770, ss1968249529, ss2028710617, ss2157123360, ss2628848060, ss2701629484, ss2710831001, ss2941921924, ss3014307408, ss3021697993, ss3351403109, ss3627508429, ss3644666061, ss3652104956, ss3741455413, ss3744140358, ss3753849011, ss3788019003, ss3793006261, ss3797891188, ss3834542067, ss3840878060, ss3884253521, ss3933595618, ss5219105243, ss5658741773, ss5846295563, ss5950162329 NC_000016.9:28632020:T:G NC_000016.10:28620699:T:G (self)
90622324, 486842827, 1372751, 33749809, 107621016, 227879480, 8955556359, ss3028179016, ss3650495918, ss3699111206, ss3725555978, ss3819142935, ss3846369101, ss3977371808, ss5012333819, ss5300634234, ss5494076552, ss5603096389, ss5773783912, ss5815881407, ss5851546025, ss5898802591 NC_000016.10:28620699:T:G NC_000016.10:28620699:T:G (self)
ss10816671, ss12357592 NT_010393.13:19778868:C:C NC_000016.10:28620699:T:G (self)
ss3378064, ss24454391, ss69342944, ss76787004, ss96633271, ss104871679, ss136654067, ss136762993, ss157237952, ss410816022 NT_010393.16:28572020:T:G NC_000016.10:28620699:T:G (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 rs2411453

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