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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.

rs235751

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr20:6789067 (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
T=0.123892 (32793/264690, TOPMED)
T=0.123700 (15246/123250, ALFA)
T=0.11368 (8901/78298, PAGE_STUDY) (+ 17 more)
T=0.03511 (992/28258, 14KJPN)
T=0.03586 (601/16760, 8.3KJPN)
T=0.1170 (749/6404, 1000G_30x)
T=0.1164 (583/5008, 1000G)
T=0.1163 (521/4480, Estonian)
T=0.1053 (406/3854, ALSPAC)
T=0.1025 (380/3708, TWINSUK)
T=0.0437 (128/2930, KOREAN)
T=0.1878 (213/1134, Daghestan)
T=0.100 (100/998, GoNL)
T=0.103 (62/600, NorthernSweden)
T=0.089 (49/548, SGDP_PRJ)
T=0.133 (43/324, HapMap)
T=0.255 (55/216, Qatari)
T=0.118 (25/212, Vietnamese)
T=0.06 (3/52, Siberian)
T=0.10 (4/40, 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 123250 T=0.123700 C=0.876300, G=0.000000
European Sub 106152 T=0.124953 C=0.875047, G=0.000000
African Sub 5026 T=0.1508 C=0.8492, G=0.0000
African Others Sub 180 T=0.156 C=0.844, G=0.000
African American Sub 4846 T=0.1506 C=0.8494, G=0.0000
Asian Sub 262 T=0.092 C=0.908, G=0.000
East Asian Sub 186 T=0.086 C=0.914, G=0.000
Other Asian Sub 76 T=0.11 C=0.89, G=0.00
Latin American 1 Sub 560 T=0.125 C=0.875, G=0.000
Latin American 2 Sub 5472 T=0.0793 C=0.9207, G=0.0000
South Asian Sub 80 T=0.17 C=0.82, G=0.00
Other Sub 5698 T=0.1197 C=0.8803, G=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
TopMed Global Study-wide 264690 T=0.123892 C=0.876108
Allele Frequency Aggregator Total Global 123250 T=0.123700 C=0.876300, G=0.000000
Allele Frequency Aggregator European Sub 106152 T=0.124953 C=0.875047, G=0.000000
Allele Frequency Aggregator Other Sub 5698 T=0.1197 C=0.8803, G=0.0000
Allele Frequency Aggregator Latin American 2 Sub 5472 T=0.0793 C=0.9207, G=0.0000
Allele Frequency Aggregator African Sub 5026 T=0.1508 C=0.8492, G=0.0000
Allele Frequency Aggregator Latin American 1 Sub 560 T=0.125 C=0.875, G=0.000
Allele Frequency Aggregator Asian Sub 262 T=0.092 C=0.908, G=0.000
Allele Frequency Aggregator South Asian Sub 80 T=0.17 C=0.82, G=0.00
The PAGE Study Global Study-wide 78298 T=0.11368 C=0.88632
The PAGE Study AfricanAmerican Sub 32372 T=0.14272 C=0.85728
The PAGE Study Mexican Sub 10770 T=0.08477 C=0.91523
The PAGE Study Asian Sub 8310 T=0.0409 C=0.9591
The PAGE Study PuertoRican Sub 7852 T=0.1149 C=0.8851
The PAGE Study NativeHawaiian Sub 4494 T=0.0710 C=0.9290
The PAGE Study Cuban Sub 4178 T=0.1453 C=0.8547
The PAGE Study Dominican Sub 3800 T=0.1276 C=0.8724
The PAGE Study CentralAmerican Sub 2442 T=0.1114 C=0.8886
The PAGE Study SouthAmerican Sub 1976 T=0.0860 C=0.9140
The PAGE Study NativeAmerican Sub 1254 T=0.0933 C=0.9067
The PAGE Study SouthAsian Sub 850 T=0.184 C=0.816
14KJPN JAPANESE Study-wide 28258 T=0.03511 C=0.96489
8.3KJPN JAPANESE Study-wide 16760 T=0.03586 C=0.96414
1000Genomes_30x Global Study-wide 6404 T=0.1170 C=0.8830
1000Genomes_30x African Sub 1786 T=0.1333 C=0.8667
1000Genomes_30x Europe Sub 1266 T=0.1319 C=0.8681
1000Genomes_30x South Asian Sub 1202 T=0.1556 C=0.8444
1000Genomes_30x East Asian Sub 1170 T=0.0701 C=0.9299
1000Genomes_30x American Sub 980 T=0.077 C=0.923
1000Genomes Global Study-wide 5008 T=0.1164 C=0.8836
1000Genomes African Sub 1322 T=0.1392 C=0.8608
1000Genomes East Asian Sub 1008 T=0.0675 C=0.9325
1000Genomes Europe Sub 1006 T=0.1292 C=0.8708
1000Genomes South Asian Sub 978 T=0.150 C=0.850
1000Genomes American Sub 694 T=0.078 C=0.922
Genetic variation in the Estonian population Estonian Study-wide 4480 T=0.1163 C=0.8837
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 T=0.1053 C=0.8947
UK 10K study - Twins TWIN COHORT Study-wide 3708 T=0.1025 C=0.8975
KOREAN population from KRGDB KOREAN Study-wide 2930 T=0.0437 C=0.9563
Genome-wide autozygosity in Daghestan Global Study-wide 1134 T=0.1878 C=0.8122
Genome-wide autozygosity in Daghestan Daghestan Sub 628 T=0.183 C=0.817
Genome-wide autozygosity in Daghestan Near_East Sub 144 T=0.271 C=0.729
Genome-wide autozygosity in Daghestan Central Asia Sub 122 T=0.156 C=0.844
Genome-wide autozygosity in Daghestan Europe Sub 108 T=0.120 C=0.880
Genome-wide autozygosity in Daghestan South Asian Sub 98 T=0.22 C=0.78
Genome-wide autozygosity in Daghestan Caucasus Sub 34 T=0.15 C=0.85
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 T=0.100 C=0.900
Northern Sweden ACPOP Study-wide 600 T=0.103 C=0.897
SGDP_PRJ Global Study-wide 548 T=0.089 C=0.911
HapMap Global Study-wide 324 T=0.133 C=0.867
HapMap American Sub 120 T=0.150 C=0.850
HapMap African Sub 114 T=0.158 C=0.842
HapMap Asian Sub 90 T=0.08 C=0.92
Qatari Global Study-wide 216 T=0.255 C=0.745
A Vietnamese Genetic Variation Database Global Study-wide 212 T=0.118 C=0.882
Siberian Global Study-wide 52 T=0.06 C=0.94
The Danish reference pan genome Danish Study-wide 40 T=0.10 C=0.90
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 20 NC_000020.11:g.6789067T>C
GRCh38.p14 chr 20 NC_000020.11:g.6789067T>G
GRCh37.p13 chr 20 NC_000020.10:g.6769714T>C
GRCh37.p13 chr 20 NC_000020.10:g.6769714T>G
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 20 NC_000020.11:g.6789067= NC_000020.11:g.6789067T>C NC_000020.11:g.6789067T>G
GRCh37.p13 chr 20 NC_000020.10:g.6769714= NC_000020.10:g.6769714T>C NC_000020.10:g.6769714T>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#.

116 SubSNP, 22 Frequency submissions
No Submitter Submission ID Date (Build)
1 KWOK ss304278 Jul 12, 2000 (79)
2 KWOK ss1031317 Oct 04, 2000 (86)
3 KWOK ss1840285 Oct 18, 2000 (87)
4 SC_JCM ss3876535 Sep 28, 2001 (100)
5 SC_SNP ss8408125 Apr 21, 2003 (114)
6 BCM_SSAHASNP ss10970229 Jul 11, 2003 (116)
7 WI_SSAHASNP ss12496543 Jul 11, 2003 (116)
8 ABI ss41413175 Mar 14, 2006 (126)
9 HGSV ss84466173 Dec 14, 2007 (130)
10 BCMHGSC_JDW ss91628898 Mar 24, 2008 (129)
11 HUMANGENOME_JCVI ss96212411 Feb 03, 2009 (130)
12 BGI ss106177103 Feb 03, 2009 (130)
13 1000GENOMES ss111675337 Jan 25, 2009 (130)
14 1000GENOMES ss115417927 Jan 25, 2009 (130)
15 ILLUMINA-UK ss117472545 Feb 14, 2009 (130)
16 ENSEMBL ss138205519 Dec 01, 2009 (131)
17 ENSEMBL ss139583311 Dec 01, 2009 (131)
18 GMI ss156129743 Dec 01, 2009 (131)
19 ILLUMINA ss160539473 Dec 01, 2009 (131)
20 COMPLETE_GENOMICS ss167754787 Jul 04, 2010 (132)
21 COMPLETE_GENOMICS ss168995471 Jul 04, 2010 (132)
22 BUSHMAN ss203821729 Jul 04, 2010 (132)
23 BCM-HGSC-SUB ss208582304 Jul 04, 2010 (132)
24 1000GENOMES ss228240771 Jul 14, 2010 (132)
25 1000GENOMES ss237751792 Jul 15, 2010 (132)
26 1000GENOMES ss243940689 Jul 15, 2010 (132)
27 BL ss255464012 May 09, 2011 (134)
28 GMI ss283289804 May 04, 2012 (137)
29 GMI ss287417699 Apr 25, 2013 (138)
30 PJP ss292603987 May 09, 2011 (134)
31 ILLUMINA ss480543867 May 04, 2012 (137)
32 ILLUMINA ss480557924 May 04, 2012 (137)
33 ILLUMINA ss481372265 Sep 08, 2015 (146)
34 ILLUMINA ss485067775 May 04, 2012 (137)
35 ILLUMINA ss537081544 Sep 08, 2015 (146)
36 TISHKOFF ss566118542 Apr 25, 2013 (138)
37 SSMP ss661989711 Apr 25, 2013 (138)
38 ILLUMINA ss778866582 Sep 08, 2015 (146)
39 ILLUMINA ss782980154 Sep 08, 2015 (146)
40 ILLUMINA ss783941195 Sep 08, 2015 (146)
41 ILLUMINA ss832236676 Sep 08, 2015 (146)
42 ILLUMINA ss834327436 Sep 08, 2015 (146)
43 EVA-GONL ss994511602 Aug 21, 2014 (142)
44 JMKIDD_LAB ss1082050773 Aug 21, 2014 (142)
45 1000GENOMES ss1363963404 Aug 21, 2014 (142)
46 HAMMER_LAB ss1397762757 Sep 08, 2015 (146)
47 DDI ss1428987591 Apr 01, 2015 (144)
48 EVA_GENOME_DK ss1579425738 Apr 01, 2015 (144)
49 EVA_UK10K_ALSPAC ss1638356502 Apr 01, 2015 (144)
50 EVA_UK10K_TWINSUK ss1681350535 Apr 01, 2015 (144)
51 EVA_DECODE ss1698566556 Apr 01, 2015 (144)
52 ILLUMINA ss1752398264 Sep 08, 2015 (146)
53 HAMMER_LAB ss1809410624 Sep 08, 2015 (146)
54 WEILL_CORNELL_DGM ss1938021950 Feb 12, 2016 (147)
55 ILLUMINA ss1959896605 Feb 12, 2016 (147)
56 GENOMED ss1969084015 Jul 19, 2016 (147)
57 JJLAB ss2029789100 Sep 14, 2016 (149)
58 USC_VALOUEV ss2158343477 Dec 20, 2016 (150)
59 HUMAN_LONGEVITY ss2241113715 Dec 20, 2016 (150)
60 SYSTEMSBIOZJU ss2629391854 Nov 08, 2017 (151)
61 ILLUMINA ss2633773463 Nov 08, 2017 (151)
62 GRF ss2704016074 Nov 08, 2017 (151)
63 GNOMAD ss2965152836 Nov 08, 2017 (151)
64 SWEGEN ss3017827996 Nov 08, 2017 (151)
65 ILLUMINA ss3022098725 Nov 08, 2017 (151)
66 BIOINF_KMB_FNS_UNIBA ss3028727109 Nov 08, 2017 (151)
67 CSHL ss3352407007 Nov 08, 2017 (151)
68 ILLUMINA ss3628344810 Oct 12, 2018 (152)
69 ILLUMINA ss3631731406 Oct 12, 2018 (152)
70 ILLUMINA ss3633243257 Oct 12, 2018 (152)
71 ILLUMINA ss3633957016 Oct 12, 2018 (152)
72 ILLUMINA ss3634825325 Oct 12, 2018 (152)
73 ILLUMINA ss3635642255 Oct 12, 2018 (152)
74 ILLUMINA ss3636515578 Oct 12, 2018 (152)
75 ILLUMINA ss3637394323 Oct 12, 2018 (152)
76 ILLUMINA ss3640532623 Oct 12, 2018 (152)
77 ILLUMINA ss3641124653 Oct 12, 2018 (152)
78 ILLUMINA ss3641420827 Oct 12, 2018 (152)
79 URBANLAB ss3650965542 Oct 12, 2018 (152)
80 ILLUMINA ss3652553003 Oct 12, 2018 (152)
81 EGCUT_WGS ss3684542304 Jul 13, 2019 (153)
82 EVA_DECODE ss3706509778 Jul 13, 2019 (153)
83 ILLUMINA ss3725898037 Jul 13, 2019 (153)
84 ACPOP ss3743226559 Jul 13, 2019 (153)
85 ILLUMINA ss3745125215 Jul 13, 2019 (153)
86 EVA ss3758390539 Jul 13, 2019 (153)
87 PAGE_CC ss3772034832 Jul 13, 2019 (153)
88 ILLUMINA ss3772621493 Jul 13, 2019 (153)
89 PACBIO ss3788592816 Jul 13, 2019 (153)
90 PACBIO ss3793494054 Jul 13, 2019 (153)
91 PACBIO ss3798381187 Jul 13, 2019 (153)
92 KHV_HUMAN_GENOMES ss3821563094 Jul 13, 2019 (153)
93 EVA ss3835574331 Apr 27, 2020 (154)
94 EVA ss3841411465 Apr 27, 2020 (154)
95 EVA ss3846919062 Apr 27, 2020 (154)
96 SGDP_PRJ ss3888679053 Apr 27, 2020 (154)
97 KRGDB ss3938866222 Apr 27, 2020 (154)
98 TOPMED ss5081380402 Apr 26, 2021 (155)
99 TOMMO_GENOMICS ss5228732430 Apr 26, 2021 (155)
100 1000G_HIGH_COVERAGE ss5307998746 Oct 13, 2022 (156)
101 EVA ss5315992487 Oct 13, 2022 (156)
102 EVA ss5436096655 Oct 13, 2022 (156)
103 HUGCELL_USP ss5500406493 Oct 13, 2022 (156)
104 1000G_HIGH_COVERAGE ss5614032913 Oct 13, 2022 (156)
105 SANFORD_IMAGENETICS ss5624479822 Oct 13, 2022 (156)
106 SANFORD_IMAGENETICS ss5662813768 Oct 13, 2022 (156)
107 TOMMO_GENOMICS ss5787690753 Oct 13, 2022 (156)
108 EVA ss5800015286 Oct 13, 2022 (156)
109 YY_MCH ss5817794369 Oct 13, 2022 (156)
110 EVA ss5845409558 Oct 13, 2022 (156)
111 EVA ss5847501834 Oct 13, 2022 (156)
112 EVA ss5847913560 Oct 13, 2022 (156)
113 EVA ss5853057028 Oct 13, 2022 (156)
114 EVA ss5922572184 Oct 13, 2022 (156)
115 EVA ss5957712879 Oct 13, 2022 (156)
116 EVA ss5979609354 Oct 13, 2022 (156)
117 1000Genomes NC_000020.10 - 6769714 Oct 12, 2018 (152)
118 1000Genomes_30x NC_000020.11 - 6789067 Oct 13, 2022 (156)
119 The Avon Longitudinal Study of Parents and Children NC_000020.10 - 6769714 Oct 12, 2018 (152)
120 Genome-wide autozygosity in Daghestan NC_000020.9 - 6717714 Apr 27, 2020 (154)
121 Genetic variation in the Estonian population NC_000020.10 - 6769714 Oct 12, 2018 (152)
122 The Danish reference pan genome NC_000020.10 - 6769714 Apr 27, 2020 (154)
123 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 545765965 (NC_000020.11:6789066:T:C 122641/140230)
Row 545765966 (NC_000020.11:6789066:T:G 1/140252)

- Apr 26, 2021 (155)
124 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 545765965 (NC_000020.11:6789066:T:C 122641/140230)
Row 545765966 (NC_000020.11:6789066:T:G 1/140252)

- Apr 26, 2021 (155)
125 Genome of the Netherlands Release 5 NC_000020.10 - 6769714 Apr 27, 2020 (154)
126 HapMap NC_000020.11 - 6789067 Apr 27, 2020 (154)
127 KOREAN population from KRGDB NC_000020.10 - 6769714 Apr 27, 2020 (154)
128 Northern Sweden NC_000020.10 - 6769714 Jul 13, 2019 (153)
129 The PAGE Study NC_000020.11 - 6789067 Jul 13, 2019 (153)
130 Qatari NC_000020.10 - 6769714 Apr 27, 2020 (154)
131 SGDP_PRJ NC_000020.10 - 6769714 Apr 27, 2020 (154)
132 Siberian NC_000020.10 - 6769714 Apr 27, 2020 (154)
133 8.3KJPN NC_000020.10 - 6769714 Apr 26, 2021 (155)
134 14KJPN NC_000020.11 - 6789067 Oct 13, 2022 (156)
135 TopMed NC_000020.11 - 6789067 Apr 26, 2021 (155)
136 UK 10K study - Twins NC_000020.10 - 6769714 Oct 12, 2018 (152)
137 A Vietnamese Genetic Variation Database NC_000020.10 - 6769714 Jul 13, 2019 (153)
138 ALFA NC_000020.11 - 6789067 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)
rs56919934 May 23, 2008 (130)
rs386565559 Aug 21, 2014 (142)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
276947, ss84466173, ss91628898, ss111675337, ss115417927, ss117472545, ss160539473, ss167754787, ss168995471, ss203821729, ss208582304, ss255464012, ss283289804, ss287417699, ss292603987, ss480543867, ss1397762757, ss1698566556 NC_000020.9:6717713:T:C NC_000020.11:6789066:T:C (self)
77399407, 42844060, 30280552, 5590677, 19090241, 46043616, 16511424, 20063872, 40696033, 10859831, 86701737, 42844060, 9458010, ss228240771, ss237751792, ss243940689, ss480557924, ss481372265, ss485067775, ss537081544, ss566118542, ss661989711, ss778866582, ss782980154, ss783941195, ss832236676, ss834327436, ss994511602, ss1082050773, ss1363963404, ss1428987591, ss1579425738, ss1638356502, ss1681350535, ss1752398264, ss1809410624, ss1938021950, ss1959896605, ss1969084015, ss2029789100, ss2158343477, ss2629391854, ss2633773463, ss2704016074, ss2965152836, ss3017827996, ss3022098725, ss3352407007, ss3628344810, ss3631731406, ss3633243257, ss3633957016, ss3634825325, ss3635642255, ss3636515578, ss3637394323, ss3640532623, ss3641124653, ss3641420827, ss3652553003, ss3684542304, ss3743226559, ss3745125215, ss3758390539, ss3772621493, ss3788592816, ss3793494054, ss3798381187, ss3835574331, ss3841411465, ss3888679053, ss3938866222, ss5228732430, ss5315992487, ss5436096655, ss5624479822, ss5662813768, ss5800015286, ss5845409558, ss5847501834, ss5847913560, ss5957712879, ss5979609354 NC_000020.10:6769713:T:C NC_000020.11:6789066:T:C (self)
101558848, 2062195, 1256301, 121527857, 356489347, 9819650316, ss2241113715, ss3028727109, ss3650965542, ss3706509778, ss3725898037, ss3772034832, ss3821563094, ss3846919062, ss5081380402, ss5307998746, ss5500406493, ss5614032913, ss5787690753, ss5817794369, ss5853057028, ss5922572184 NC_000020.11:6789066:T:C NC_000020.11:6789066:T:C (self)
ss304278, ss1031317, ss1840285, ss3876535, ss8408125, ss10970229, ss12496543, ss41413175, ss96212411, ss106177103, ss138205519, ss139583311, ss156129743 NT_011387.8:6709713:T:C NC_000020.11:6789066:T:C (self)
9819650316 NC_000020.11:6789066:T:G NC_000020.11:6789066: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 rs235751

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