Skip to main page content
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.

rs1042157

Current Build 155

Released April 9, 2021

Organism
Homo sapiens
Position
chr16:28605736 (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
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.345809 (47835/138328, GnomAD)
A=0.32963 (9467/28720, ALFA)
A=0.20859 (3496/16760, 8.3KJPN) (+ 14 more)
A=0.2911 (1458/5008, 1000G)
A=0.3918 (1510/3854, ALSPAC)
A=0.3900 (1446/3708, TWINSUK)
A=0.2037 (596/2926, KOREAN)
A=0.1989 (364/1830, Korea1K)
A=0.375 (374/998, GoNL)
A=0.255 (201/788, PRJEB37584)
A=0.431 (257/596, NorthernSweden)
A=0.301 (161/534, MGP)
G=0.367 (119/324, SGDP_PRJ)
A=0.238 (51/214, Qatari)
A=0.224 (48/214, Vietnamese)
A=0.163 (33/202, HapMap)
G=0.42 (16/38, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
SULT1A1 : Non Coding Transcript Variant
Publications
5 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: 20201027095038
Population Group Sample Size Ref Allele Alt Allele
Total Global 28720 G=0.67037 A=0.32963, C=0.00000
European Sub 25174 G=0.64181 A=0.35819, C=0.00000
African Sub 1884 G=0.9124 A=0.0876, C=0.0000
African Others Sub 82 G=0.93 A=0.07, C=0.00
African American Sub 1802 G=0.9118 A=0.0882, C=0.0000
Asian Sub 66 G=1.00 A=0.00, C=0.00
East Asian Sub 50 G=1.00 A=0.00, C=0.00
Other Asian Sub 16 G=1.00 A=0.00, C=0.00
Latin American 1 Sub 76 G=1.00 A=0.00, C=0.00
Latin American 2 Sub 172 G=1.000 A=0.000, C=0.000
South Asian Sub 58 G=1.00 A=0.00, C=0.00
Other Sub 1290 G=0.7791 A=0.2209, C=0.0000


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
gnomAD - Genomes Global Study-wide 138328 G=0.654191 A=0.345809
gnomAD - Genomes European Sub 75024 G=0.59824 A=0.40176
gnomAD - Genomes African Sub 41458 G=0.76118 A=0.23882
gnomAD - Genomes American Sub 13454 G=0.59848 A=0.40152
gnomAD - Genomes Ashkenazi Jewish Sub 3294 G=0.7010 A=0.2990
gnomAD - Genomes East Asian Sub 2992 G=0.7604 A=0.2396
gnomAD - Genomes Other Sub 2106 G=0.6733 A=0.3267
Allele Frequency Aggregator Total Global 28720 G=0.67037 A=0.32963, C=0.00000
Allele Frequency Aggregator European Sub 25174 G=0.64181 A=0.35819, C=0.00000
Allele Frequency Aggregator African Sub 1884 G=0.9124 A=0.0876, C=0.0000
Allele Frequency Aggregator Other Sub 1290 G=0.7791 A=0.2209, C=0.0000
Allele Frequency Aggregator Latin American 2 Sub 172 G=1.000 A=0.000, C=0.000
Allele Frequency Aggregator Latin American 1 Sub 76 G=1.00 A=0.00, C=0.00
Allele Frequency Aggregator Asian Sub 66 G=1.00 A=0.00, C=0.00
Allele Frequency Aggregator South Asian Sub 58 G=1.00 A=0.00, C=0.00
8.3KJPN JAPANESE Study-wide 16760 G=0.79141 A=0.20859
1000Genomes Global Study-wide 5008 G=0.7089 A=0.2911
1000Genomes African Sub 1322 G=0.7716 A=0.2284
1000Genomes East Asian Sub 1008 G=0.7341 A=0.2659
1000Genomes Europe Sub 1006 G=0.6650 A=0.3350
1000Genomes South Asian Sub 978 G=0.775 A=0.225
1000Genomes American Sub 694 G=0.523 A=0.477
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.6082 A=0.3918
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.6100 A=0.3900
KOREAN population from KRGDB KOREAN Study-wide 2926 G=0.7963 A=0.2037
Korean Genome Project KOREAN Study-wide 1830 G=0.8011 A=0.1989
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.625 A=0.375
CNV burdens in cranial meningiomas Global Study-wide 788 G=0.745 A=0.255
CNV burdens in cranial meningiomas CRM Sub 788 G=0.745 A=0.255
Northern Sweden ACPOP Study-wide 596 G=0.569 A=0.431
Medical Genome Project healthy controls from Spanish population Spanish controls Study-wide 534 G=0.699 A=0.301
SGDP_PRJ Global Study-wide 324 G=0.367 A=0.633
Qatari Global Study-wide 214 G=0.762 A=0.238
A Vietnamese Genetic Variation Database Global Study-wide 214 G=0.776 A=0.224
HapMap Global Study-wide 202 G=0.837 A=0.163
HapMap African Sub 114 G=0.877 A=0.123
HapMap Asian Sub 88 G=0.78 A=0.22
Siberian Global Study-wide 38 G=0.42 A=0.58
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 16 NC_000016.10:g.28605736G>A
GRCh38.p13 chr 16 NC_000016.10:g.28605736G>C
GRCh37.p13 chr 16 NC_000016.9:g.28617057G>A
GRCh37.p13 chr 16 NC_000016.9:g.28617057G>C
SULT1A1 RefSeqGene NG_028128.1:g.22810C>T
SULT1A1 RefSeqGene NG_028128.1:g.22810C>G
Gene: SULT1A1, sulfotransferase family 1A member 1 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
SULT1A1 transcript variant 1 NM_001055.3:c.*85= N/A 3 Prime UTR Variant
SULT1A1 transcript variant 2 NM_177529.2:c.*85= N/A 3 Prime UTR Variant
SULT1A1 transcript variant 3 NM_177530.3:c.*85= N/A 3 Prime UTR Variant
SULT1A1 transcript variant 5 NM_177536.4:c.*85= N/A 3 Prime UTR Variant
SULT1A1 transcript variant 4 NM_177534.3:c.*85= N/A 3 Prime UTR Variant
SULT1A1 transcript variant X1 XM_017023604.1:c.*85= N/A 3 Prime UTR Variant
SULT1A1 transcript variant X2 XM_017023605.1:c.*85= N/A 3 Prime UTR Variant
SULT1A1 transcript variant X6 XM_017023608.1:c.*85= N/A 3 Prime UTR Variant
SULT1A1 transcript variant X7 XM_017023609.1:c.*85= N/A 3 Prime UTR Variant
SULT1A1 transcript variant X8 XM_017023610.1:c.*85= N/A 3 Prime UTR Variant
SULT1A1 transcript variant X3 XM_024450408.1:c.*85= N/A 3 Prime UTR Variant
SULT1A1 transcript variant X4 XM_017023607.2:c.*85= N/A 3 Prime UTR Variant
SULT1A1 transcript variant X9 XM_017023611.2:c.*85= N/A 3 Prime UTR Variant
SULT1A1 transcript variant X10 XM_017023612.2:c.*85= N/A 3 Prime UTR Variant
SULT1A1 transcript variant X11 XM_024450409.1:c.*85= N/A 3 Prime UTR Variant
SULT1A1 transcript variant X12 XM_024450410.1:c.*85= N/A 3 Prime UTR Variant
SULT1A1 transcript variant X13 XM_024450411.1:c.*85= N/A 3 Prime UTR Variant
SULT1A1 transcript variant X14 XM_017023613.2:c.*85= N/A 3 Prime UTR Variant
SULT1A1 transcript variant X5 XR_001751973.1:n.1214C>T N/A Non Coding Transcript Variant
SULT1A1 transcript variant X5 XR_001751973.1:n.1214C>G 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.p13 chr 16 NC_000016.10:g.28605736= NC_000016.10:g.28605736G>A NC_000016.10:g.28605736G>C
GRCh37.p13 chr 16 NC_000016.9:g.28617057= NC_000016.9:g.28617057G>A NC_000016.9:g.28617057G>C
SULT1A1 RefSeqGene NG_028128.1:g.22810= NG_028128.1:g.22810C>T NG_028128.1:g.22810C>G
SULT1A1 transcript variant 5 NM_177536.4:c.*85= NM_177536.4:c.*85C>T NM_177536.4:c.*85C>G
SULT1A1 transcript variant 5 NM_177536.3:c.*85= NM_177536.3:c.*85C>T NM_177536.3:c.*85C>G
SULT1A1 transcript variant 4 NM_177534.3:c.*85= NM_177534.3:c.*85C>T NM_177534.3:c.*85C>G
SULT1A1 transcript variant 4 NM_177534.2:c.*85= NM_177534.2:c.*85C>T NM_177534.2:c.*85C>G
SULT1A1 transcript variant 3 NM_177530.3:c.*85= NM_177530.3:c.*85C>T NM_177530.3:c.*85C>G
SULT1A1 transcript variant 3 NM_177530.2:c.*85= NM_177530.2:c.*85C>T NM_177530.2:c.*85C>G
SULT1A1 transcript variant 1 NM_001055.3:c.*85= NM_001055.3:c.*85C>T NM_001055.3:c.*85C>G
SULT1A1 transcript variant 2 NM_177529.2:c.*85= NM_177529.2:c.*85C>T NM_177529.2:c.*85C>G
SULT1A1 transcript variant X9 XM_017023611.2:c.*85= XM_017023611.2:c.*85C>T XM_017023611.2:c.*85C>G
SULT1A1 transcript variant X4 XM_017023607.2:c.*85= XM_017023607.2:c.*85C>T XM_017023607.2:c.*85C>G
SULT1A1 transcript variant X10 XM_017023612.2:c.*85= XM_017023612.2:c.*85C>T XM_017023612.2:c.*85C>G
SULT1A1 transcript variant X14 XM_017023613.2:c.*85= XM_017023613.2:c.*85C>T XM_017023613.2:c.*85C>G
SULT1A1 transcript variant X11 XM_024450409.1:c.*85= XM_024450409.1:c.*85C>T XM_024450409.1:c.*85C>G
SULT1A1 transcript variant X13 XM_024450411.1:c.*85= XM_024450411.1:c.*85C>T XM_024450411.1:c.*85C>G
SULT1A1 transcript variant X12 XM_024450410.1:c.*85= XM_024450410.1:c.*85C>T XM_024450410.1:c.*85C>G
SULT1A1 transcript variant X3 XM_024450408.1:c.*85= XM_024450408.1:c.*85C>T XM_024450408.1:c.*85C>G
SULT1A1 transcript variant X5 XR_001751973.1:n.1214= XR_001751973.1:n.1214C>T XR_001751973.1:n.1214C>G
SULT1A1 transcript variant X1 XM_017023604.1:c.*85= XM_017023604.1:c.*85C>T XM_017023604.1:c.*85C>G
SULT1A1 transcript variant X2 XM_017023605.1:c.*85= XM_017023605.1:c.*85C>T XM_017023605.1:c.*85C>G
SULT1A1 transcript variant X8 XM_017023610.1:c.*85= XM_017023610.1:c.*85C>T XM_017023610.1:c.*85C>G
SULT1A1 transcript variant X7 XM_017023609.1:c.*85= XM_017023609.1:c.*85C>T XM_017023609.1:c.*85C>G
SULT1A1 transcript variant X6 XM_017023608.1:c.*85= XM_017023608.1:c.*85C>T XM_017023608.1:c.*85C>G
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#.

69 SubSNP, 17 Frequency submissions
No Submitter Submission ID Date (Build)
1 LEE ss1509123 Oct 05, 2000 (86)
2 SC_JCM ss4126325 Nov 05, 2001 (101)
3 LEE ss4390584 May 29, 2002 (108)
4 LEE ss4403428 May 29, 2002 (108)
5 RIKENSNPRC ss5603975 Dec 12, 2002 (110)
6 SNP500CANCER ss12675655 Nov 17, 2003 (118)
7 CGM_KYOTO ss76861132 Dec 06, 2007 (129)
8 BCMHGSC_JDW ss90361588 Mar 24, 2008 (129)
9 BGI ss103289930 Feb 20, 2009 (130)
10 KRIBB_YJKIM ss104798449 Feb 05, 2009 (130)
11 1000GENOMES ss109293926 Jan 23, 2009 (130)
12 ENSEMBL ss136653984 Dec 01, 2009 (131)
13 ILLUMINA ss159122954 Dec 01, 2009 (131)
14 ILLUMINA ss159891980 Dec 01, 2009 (131)
15 COMPLETE_GENOMICS ss168100900 Jul 04, 2010 (132)
16 ILLUMINA ss169093669 Jul 04, 2010 (132)
17 COMPLETE_GENOMICS ss171160885 Jul 04, 2010 (132)
18 BUSHMAN ss201601057 Jul 04, 2010 (132)
19 1000GENOMES ss227211475 Jul 14, 2010 (132)
20 1000GENOMES ss237002462 Jul 15, 2010 (132)
21 1000GENOMES ss243346911 Jul 15, 2010 (132)
22 BL ss255613580 May 09, 2011 (134)
23 GMI ss282489750 May 04, 2012 (137)
24 GMI ss287057469 Apr 25, 2013 (138)
25 ILLUMINA ss410815968 Sep 17, 2011 (135)
26 ILLUMINA ss479633759 Sep 08, 2015 (146)
27 ILLUMINA ss532746463 Sep 08, 2015 (146)
28 TISHKOFF ss564864731 Apr 25, 2013 (138)
29 SSMP ss660616910 Apr 25, 2013 (138)
30 ILLUMINA ss832635673 Jul 13, 2019 (153)
31 EVA-GONL ss992420604 Aug 21, 2014 (142)
32 JMKIDD_LAB ss1080583559 Aug 21, 2014 (142)
33 1000GENOMES ss1355922397 Aug 21, 2014 (142)
34 DDI ss1427820558 Apr 01, 2015 (144)
35 EVA_UK10K_ALSPAC ss1634284075 Apr 01, 2015 (144)
36 EVA_UK10K_TWINSUK ss1677278108 Apr 01, 2015 (144)
37 EVA_MGP ss1711424193 Apr 01, 2015 (144)
38 WEILL_CORNELL_DGM ss1935844487 Feb 12, 2016 (147)
39 ILLUMINA ss1946412981 Feb 12, 2016 (147)
40 ILLUMINA ss1959671727 Feb 12, 2016 (147)
41 GENOMED ss1968249493 Jul 19, 2016 (147)
42 JJLAB ss2028710542 Sep 14, 2016 (149)
43 ILLUMINA ss2094889163 Dec 20, 2016 (150)
44 USC_VALOUEV ss2157123268 Dec 20, 2016 (150)
45 SYSTEMSBIOZJU ss2628847998 Nov 08, 2017 (151)
46 ILLUMINA ss2633310702 Nov 08, 2017 (151)
47 GRF ss2701629340 Nov 08, 2017 (151)
48 GNOMAD ss2941920409 Nov 08, 2017 (151)
49 SWEGEN ss3014307081 Nov 08, 2017 (151)
50 BIOINF_KMB_FNS_UNIBA ss3028178964 Nov 08, 2017 (151)
51 TOPMED ss3243767431 Nov 08, 2017 (151)
52 CSHL ss3351403011 Nov 08, 2017 (151)
53 ILLUMINA ss3627508410 Oct 12, 2018 (152)
54 ILLUMINA ss3636329277 Oct 12, 2018 (152)
55 ILLUMINA ss3638121286 Oct 12, 2018 (152)
56 ILLUMINA ss3644666051 Oct 12, 2018 (152)
57 OMUKHERJEE_ADBS ss3646490107 Oct 12, 2018 (152)
58 EVA_DECODE ss3699110946 Jul 13, 2019 (153)
59 ACPOP ss3741455277 Jul 13, 2019 (153)
60 EVA ss3753848853 Jul 13, 2019 (153)
61 KHV_HUMAN_GENOMES ss3819142749 Jul 13, 2019 (153)
62 EVA ss3834541980 Apr 27, 2020 (154)
63 SGDP_PRJ ss3884253146 Apr 27, 2020 (154)
64 KRGDB ss3933595186 Apr 27, 2020 (154)
65 KOGIC ss3977371448 Apr 27, 2020 (154)
66 FSA-LAB ss3984091381 Apr 27, 2021 (155)
67 EVA ss3984711950 Apr 27, 2021 (155)
68 EVA ss3986070366 Apr 27, 2021 (155)
69 TOMMO_GENOMICS ss5219104423 Apr 27, 2021 (155)
70 1000Genomes NC_000016.9 - 28617057 Oct 12, 2018 (152)
71 The Avon Longitudinal Study of Parents and Children NC_000016.9 - 28617057 Oct 12, 2018 (152)
72 gnomAD - Genomes NC_000016.10 - 28605736 Apr 27, 2021 (155)
73 Genome of the Netherlands Release 5 NC_000016.9 - 28617057 Apr 27, 2020 (154)
74 HapMap NC_000016.10 - 28605736 Apr 27, 2020 (154)
75 KOREAN population from KRGDB NC_000016.9 - 28617057 Apr 27, 2020 (154)
76 Korean Genome Project NC_000016.10 - 28605736 Apr 27, 2020 (154)
77 Medical Genome Project healthy controls from Spanish population NC_000016.9 - 28617057 Apr 27, 2020 (154)
78 Northern Sweden NC_000016.9 - 28617057 Jul 13, 2019 (153)
79 CNV burdens in cranial meningiomas NC_000016.9 - 28617057 Apr 27, 2021 (155)
80 Qatari NC_000016.9 - 28617057 Apr 27, 2020 (154)
81 SGDP_PRJ NC_000016.9 - 28617057 Apr 27, 2020 (154)
82 Siberian NC_000016.9 - 28617057 Apr 27, 2020 (154)
83 8.3KJPN NC_000016.9 - 28617057 Apr 27, 2021 (155)
84 UK 10K study - Twins NC_000016.9 - 28617057 Oct 12, 2018 (152)
85 A Vietnamese Genetic Variation Database NC_000016.9 - 28617057 Jul 13, 2019 (153)
86 ALFA NC_000016.10 - 28605736 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)
rs1801093 Jan 18, 2001 (92)
rs3169480 Oct 08, 2002 (108)
rs117148001 Aug 16, 2010 (132)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss90361588, ss109293926, ss168100900, ss171160885, ss201601057, ss255613580, ss282489750, ss287057469, ss2094889163 NC_000016.8:28524557:G:A NC_000016.10:28605735:G:A (self)
69075429, 38346775, 17104301, 40772580, 539953, 14740142, 261484, 17886409, 36270126, 9639622, 77073730, 38346775, 8514924, ss227211475, ss237002462, ss243346911, ss479633759, ss532746463, ss564864731, ss660616910, ss832635673, ss992420604, ss1080583559, ss1355922397, ss1427820558, ss1634284075, ss1677278108, ss1711424193, ss1935844487, ss1946412981, ss1959671727, ss1968249493, ss2028710542, ss2157123268, ss2628847998, ss2633310702, ss2701629340, ss2941920409, ss3014307081, ss3351403011, ss3627508410, ss3636329277, ss3638121286, ss3644666051, ss3646490107, ss3741455277, ss3753848853, ss3834541980, ss3884253146, ss3933595186, ss3984091381, ss3984711950, ss3986070366, ss5219104423 NC_000016.9:28617056:G:A NC_000016.10:28605735:G:A (self)
486839515, 1372738, 33749449, 5728070820, ss3028178964, ss3243767431, ss3699110946, ss3819142749, ss3977371448 NC_000016.10:28605735:G:A NC_000016.10:28605735:G:A (self)
ss1509123, ss4126325, ss4390584, ss4403428, ss5603975, ss12675655, ss76861132, ss103289930, ss104798449, ss136653984, ss159122954, ss159891980, ss169093669, ss410815968 NT_010393.16:28557056:G:A NC_000016.10:28605735:G:A (self)
ss201601057 NC_000016.8:28524557:G:C NC_000016.10:28605735:G:C (self)
5728070820 NC_000016.10:28605735:G:C NC_000016.10:28605735:G:C
Help

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

5 citations for rs1042157
PMID Title Author Year Journal
20881232 Functional genetic variants in the 3'-untranslated region of sulfotransferase isoform 1A1 (SULT1A1) and their effect on enzymatic activity. Yu X et al. 2010 Toxicological sciences
21072184 Flavopiridol pharmacogenetics: clinical and functional evidence for the role of SLCO1B1/OATP1B1 in flavopiridol disposition. Ni W et al. 2010 PloS one
27713515 The influence of single nucleotide polymorphisms on the association between dietary acrylamide intake and endometrial cancer risk. Hogervorst JG et al. 2016 Scientific reports
30068618 Cohort Profile: the Predictors of Breast Cancer Recurrence (ProBe CaRE) Premenopausal Breast Cancer Cohort Study in Denmark. Collin LJ et al. 2018 BMJ open
30120701 Genetic polymorphisms of 3'-untranslated region of SULT1A1 and their impact on tamoxifen metabolism and efficacy. Sanchez-Spitman AB et al. 2018 Breast cancer research and treatment
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.post676+237644a