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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.

rs11966072

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr6:109313625 (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
A>G
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.311448 (107221/344266, ALFA)
G=0.237980 (62991/264690, TOPMED)
G=0.262223 (36740/140110, GnomAD) (+ 19 more)
G=0.16574 (13043/78694, PAGE_STUDY)
G=0.09551 (2699/28258, 14KJPN)
G=0.09696 (1625/16760, 8.3KJPN)
G=0.1699 (1088/6404, 1000G_30x)
G=0.1671 (837/5008, 1000G)
G=0.3734 (1673/4480, Estonian)
G=0.3433 (1323/3854, ALSPAC)
G=0.3287 (1219/3708, TWINSUK)
G=0.1211 (354/2922, KOREAN)
G=0.1651 (344/2084, HGDP_Stanford)
G=0.1628 (308/1892, HapMap)
G=0.343 (342/998, GoNL)
G=0.368 (221/600, NorthernSweden)
G=0.204 (44/216, Qatari)
G=0.080 (17/212, Vietnamese)
A=0.438 (63/144, SGDP_PRJ)
G=0.25 (10/40, GENOME_DK)
G=0.36 (10/28, Ancient Sardinia)
A=0.45 (9/20, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
CCDC162P : Intron Variant
Publications
2 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 349518 A=0.689089 G=0.310911
European Sub 302490 A=0.670035 G=0.329965
African Sub 9610 A=0.8748 G=0.1252
African Others Sub 372 A=0.927 G=0.073
African American Sub 9238 A=0.8727 G=0.1273
Asian Sub 6920 A=0.8828 G=0.1172
East Asian Sub 4982 A=0.8796 G=0.1204
Other Asian Sub 1938 A=0.8911 G=0.1089
Latin American 1 Sub 1134 A=0.7416 G=0.2584
Latin American 2 Sub 7224 A=0.8270 G=0.1730
South Asian Sub 5224 A=0.8338 G=0.1662
Other Sub 16916 A=0.73794 G=0.26206


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
Allele Frequency Aggregator Total Global 344266 A=0.688552 G=0.311448
Allele Frequency Aggregator European Sub 299216 A=0.670151 G=0.329849
Allele Frequency Aggregator Other Sub 16094 A=0.73599 G=0.26401
Allele Frequency Aggregator African Sub 8454 A=0.8753 G=0.1247
Allele Frequency Aggregator Latin American 2 Sub 7224 A=0.8270 G=0.1730
Allele Frequency Aggregator Asian Sub 6920 A=0.8828 G=0.1172
Allele Frequency Aggregator South Asian Sub 5224 A=0.8338 G=0.1662
Allele Frequency Aggregator Latin American 1 Sub 1134 A=0.7416 G=0.2584
TopMed Global Study-wide 264690 A=0.762020 G=0.237980
gnomAD - Genomes Global Study-wide 140110 A=0.737777 G=0.262223
gnomAD - Genomes European Sub 75854 A=0.64894 G=0.35106
gnomAD - Genomes African Sub 42008 A=0.87169 G=0.12831
gnomAD - Genomes American Sub 13638 A=0.78919 G=0.21081
gnomAD - Genomes Ashkenazi Jewish Sub 3322 A=0.7258 G=0.2742
gnomAD - Genomes East Asian Sub 3134 A=0.8835 G=0.1165
gnomAD - Genomes Other Sub 2154 A=0.7354 G=0.2646
The PAGE Study Global Study-wide 78694 A=0.83426 G=0.16574
The PAGE Study AfricanAmerican Sub 32510 A=0.86506 G=0.13494
The PAGE Study Mexican Sub 10810 A=0.84015 G=0.15985
The PAGE Study Asian Sub 8318 A=0.8922 G=0.1078
The PAGE Study PuertoRican Sub 7918 A=0.7804 G=0.2196
The PAGE Study NativeHawaiian Sub 4534 A=0.7230 G=0.2770
The PAGE Study Cuban Sub 4230 A=0.7357 G=0.2643
The PAGE Study Dominican Sub 3826 A=0.8061 G=0.1939
The PAGE Study CentralAmerican Sub 2450 A=0.8388 G=0.1612
The PAGE Study SouthAmerican Sub 1982 A=0.8375 G=0.1625
The PAGE Study NativeAmerican Sub 1260 A=0.7381 G=0.2619
The PAGE Study SouthAsian Sub 856 A=0.849 G=0.151
14KJPN JAPANESE Study-wide 28258 A=0.90449 G=0.09551
8.3KJPN JAPANESE Study-wide 16760 A=0.90304 G=0.09696
1000Genomes_30x Global Study-wide 6404 A=0.8301 G=0.1699
1000Genomes_30x African Sub 1786 A=0.8987 G=0.1013
1000Genomes_30x Europe Sub 1266 A=0.6603 G=0.3397
1000Genomes_30x South Asian Sub 1202 A=0.8619 G=0.1381
1000Genomes_30x East Asian Sub 1170 A=0.8778 G=0.1222
1000Genomes_30x American Sub 980 A=0.829 G=0.171
1000Genomes Global Study-wide 5008 A=0.8329 G=0.1671
1000Genomes African Sub 1322 A=0.9002 G=0.0998
1000Genomes East Asian Sub 1008 A=0.8800 G=0.1200
1000Genomes Europe Sub 1006 A=0.6690 G=0.3310
1000Genomes South Asian Sub 978 A=0.868 G=0.132
1000Genomes American Sub 694 A=0.824 G=0.176
Genetic variation in the Estonian population Estonian Study-wide 4480 A=0.6266 G=0.3734
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 A=0.6567 G=0.3433
UK 10K study - Twins TWIN COHORT Study-wide 3708 A=0.6713 G=0.3287
KOREAN population from KRGDB KOREAN Study-wide 2922 A=0.8789 G=0.1211
HGDP-CEPH-db Supplement 1 Global Study-wide 2084 A=0.8349 G=0.1651
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 A=0.885 G=0.115
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 A=0.843 G=0.157
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 A=0.771 G=0.229
HGDP-CEPH-db Supplement 1 Europe Sub 320 A=0.659 G=0.341
HGDP-CEPH-db Supplement 1 Africa Sub 242 A=0.888 G=0.112
HGDP-CEPH-db Supplement 1 America Sub 216 A=0.977 G=0.023
HGDP-CEPH-db Supplement 1 Oceania Sub 72 A=0.94 G=0.06
HapMap Global Study-wide 1892 A=0.8372 G=0.1628
HapMap American Sub 770 A=0.809 G=0.191
HapMap African Sub 692 A=0.857 G=0.143
HapMap Asian Sub 254 A=0.921 G=0.079
HapMap Europe Sub 176 A=0.761 G=0.239
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 A=0.657 G=0.343
Northern Sweden ACPOP Study-wide 600 A=0.632 G=0.368
Qatari Global Study-wide 216 A=0.796 G=0.204
A Vietnamese Genetic Variation Database Global Study-wide 212 A=0.920 G=0.080
SGDP_PRJ Global Study-wide 144 A=0.438 G=0.562
The Danish reference pan genome Danish Study-wide 40 A=0.75 G=0.25
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 28 A=0.64 G=0.36
Siberian Global Study-wide 20 A=0.45 G=0.55
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 6 NC_000006.12:g.109313625A>G
GRCh37.p13 chr 6 NC_000006.11:g.109634828A>G
Gene: CCDC162P, coiled-coil domain containing 162, pseudogene (plus strand)
Molecule type Change Amino acid[Codon] SO Term
CCDC162P transcript NR_152435.1:n. N/A Intron 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 A= G
GRCh38.p14 chr 6 NC_000006.12:g.109313625= NC_000006.12:g.109313625A>G
GRCh37.p13 chr 6 NC_000006.11:g.109634828= NC_000006.11:g.109634828A>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#.

149 SubSNP, 22 Frequency submissions
No Submitter Submission ID Date (Build)
1 CSHL-HAPMAP ss17892962 Feb 28, 2004 (120)
2 SSAHASNP ss22374558 Apr 05, 2004 (121)
3 ABI ss42707515 Mar 14, 2006 (126)
4 ILLUMINA ss66971634 Dec 01, 2006 (127)
5 ILLUMINA ss67141122 Dec 01, 2006 (127)
6 ILLUMINA ss68118054 Dec 12, 2006 (127)
7 ILLUMINA ss70550251 May 25, 2008 (130)
8 ILLUMINA ss71085471 May 17, 2007 (127)
9 ILLUMINA ss75628959 Dec 07, 2007 (129)
10 HGSV ss77757665 Dec 07, 2007 (129)
11 KRIBB_YJKIM ss85166486 Dec 15, 2007 (130)
12 BCMHGSC_JDW ss93536546 Mar 24, 2008 (129)
13 HUMANGENOME_JCVI ss98422827 Feb 05, 2009 (130)
14 1000GENOMES ss110720000 Jan 25, 2009 (130)
15 1000GENOMES ss114916354 Jan 25, 2009 (130)
16 ENSEMBL ss143865867 Dec 01, 2009 (131)
17 ILLUMINA ss153102975 Dec 01, 2009 (131)
18 GMI ss157433399 Dec 01, 2009 (131)
19 ILLUMINA ss159198003 Dec 01, 2009 (131)
20 ILLUMINA ss160021710 Dec 01, 2009 (131)
21 COMPLETE_GENOMICS ss162705031 Jul 04, 2010 (132)
22 COMPLETE_GENOMICS ss164214024 Jul 04, 2010 (132)
23 ILLUMINA ss171755965 Jul 04, 2010 (132)
24 BCM-HGSC-SUB ss207364284 Jul 04, 2010 (132)
25 1000GENOMES ss222603565 Jul 14, 2010 (132)
26 1000GENOMES ss233632003 Jul 15, 2010 (132)
27 1000GENOMES ss240657129 Jul 15, 2010 (132)
28 BL ss254636733 May 09, 2011 (134)
29 GMI ss278969393 May 04, 2012 (137)
30 PJP ss293696756 May 09, 2011 (134)
31 ILLUMINA ss479640050 May 04, 2012 (137)
32 ILLUMINA ss479645309 May 04, 2012 (137)
33 ILLUMINA ss480152680 Sep 08, 2015 (146)
34 ILLUMINA ss484618700 May 04, 2012 (137)
35 EXOME_CHIP ss491390146 May 04, 2012 (137)
36 ILLUMINA ss536741803 Sep 08, 2015 (146)
37 TISHKOFF ss559442012 Apr 25, 2013 (138)
38 SSMP ss653553139 Apr 25, 2013 (138)
39 ILLUMINA ss778396277 Aug 21, 2014 (142)
40 ILLUMINA ss780681256 Aug 21, 2014 (142)
41 ILLUMINA ss782756167 Aug 21, 2014 (142)
42 ILLUMINA ss783354560 Aug 21, 2014 (142)
43 ILLUMINA ss783722710 Aug 21, 2014 (142)
44 ILLUMINA ss832008364 Apr 01, 2015 (144)
45 ILLUMINA ss832710466 Aug 21, 2014 (142)
46 ILLUMINA ss833301155 Aug 21, 2014 (142)
47 ILLUMINA ss833851396 Aug 21, 2014 (142)
48 EVA-GONL ss983358557 Aug 21, 2014 (142)
49 JMKIDD_LAB ss1073927280 Aug 21, 2014 (142)
50 1000GENOMES ss1321733469 Aug 21, 2014 (142)
51 DDI ss1430856538 Apr 01, 2015 (144)
52 EVA_GENOME_DK ss1581842377 Apr 01, 2015 (144)
53 EVA_DECODE ss1592920031 Apr 01, 2015 (144)
54 EVA_UK10K_ALSPAC ss1616408190 Apr 01, 2015 (144)
55 EVA_UK10K_TWINSUK ss1659402223 Apr 01, 2015 (144)
56 EVA_SVP ss1712890264 Apr 01, 2015 (144)
57 ILLUMINA ss1752594866 Sep 08, 2015 (146)
58 ILLUMINA ss1752594867 Sep 08, 2015 (146)
59 ILLUMINA ss1917809313 Feb 12, 2016 (147)
60 WEILL_CORNELL_DGM ss1926606709 Feb 12, 2016 (147)
61 ILLUMINA ss1946187943 Feb 12, 2016 (147)
62 ILLUMINA ss1946187944 Feb 12, 2016 (147)
63 ILLUMINA ss1958940504 Feb 12, 2016 (147)
64 ILLUMINA ss1958940505 Feb 12, 2016 (147)
65 JJLAB ss2023952805 Sep 14, 2016 (149)
66 USC_VALOUEV ss2152147510 Dec 20, 2016 (150)
67 HUMAN_LONGEVITY ss2287242901 Dec 20, 2016 (150)
68 ILLUMINA ss2634495742 Nov 08, 2017 (151)
69 ILLUMINA ss2634495743 Nov 08, 2017 (151)
70 ILLUMINA ss2634495744 Nov 08, 2017 (151)
71 GRF ss2707773906 Nov 08, 2017 (151)
72 ILLUMINA ss2711086818 Nov 08, 2017 (151)
73 GNOMAD ss2843561107 Nov 08, 2017 (151)
74 AFFY ss2985377714 Nov 08, 2017 (151)
75 AFFY ss2986010302 Nov 08, 2017 (151)
76 SWEGEN ss2999735151 Nov 08, 2017 (151)
77 ILLUMINA ss3022654685 Nov 08, 2017 (151)
78 ILLUMINA ss3022654686 Nov 08, 2017 (151)
79 BIOINF_KMB_FNS_UNIBA ss3025772208 Nov 08, 2017 (151)
80 CSHL ss3347168903 Nov 08, 2017 (151)
81 ILLUMINA ss3625909504 Oct 12, 2018 (152)
82 ILLUMINA ss3629627005 Oct 12, 2018 (152)
83 ILLUMINA ss3629627006 Oct 12, 2018 (152)
84 ILLUMINA ss3632409964 Oct 12, 2018 (152)
85 ILLUMINA ss3633433424 Oct 12, 2018 (152)
86 ILLUMINA ss3634156848 Oct 12, 2018 (152)
87 ILLUMINA ss3635082634 Oct 12, 2018 (152)
88 ILLUMINA ss3635082635 Oct 12, 2018 (152)
89 ILLUMINA ss3635837398 Oct 12, 2018 (152)
90 ILLUMINA ss3636807421 Oct 12, 2018 (152)
91 ILLUMINA ss3637590245 Oct 12, 2018 (152)
92 ILLUMINA ss3638649999 Oct 12, 2018 (152)
93 ILLUMINA ss3639325888 Oct 12, 2018 (152)
94 ILLUMINA ss3639958248 Oct 12, 2018 (152)
95 ILLUMINA ss3640789935 Oct 12, 2018 (152)
96 ILLUMINA ss3640789936 Oct 12, 2018 (152)
97 ILLUMINA ss3643589628 Oct 12, 2018 (152)
98 ILLUMINA ss3644002959 Oct 12, 2018 (152)
99 ILLUMINA ss3644921053 Oct 12, 2018 (152)
100 ILLUMINA ss3644921054 Oct 12, 2018 (152)
101 URBANLAB ss3648443368 Oct 12, 2018 (152)
102 ILLUMINA ss3653174070 Oct 12, 2018 (152)
103 ILLUMINA ss3653174071 Oct 12, 2018 (152)
104 ILLUMINA ss3654144017 Oct 12, 2018 (152)
105 EGCUT_WGS ss3667631358 Jul 13, 2019 (153)
106 EVA_DECODE ss3718013709 Jul 13, 2019 (153)
107 ILLUMINA ss3726373558 Jul 13, 2019 (153)
108 ACPOP ss3733864518 Jul 13, 2019 (153)
109 ILLUMINA ss3744276788 Jul 13, 2019 (153)
110 ILLUMINA ss3744558936 Jul 13, 2019 (153)
111 ILLUMINA ss3745382569 Jul 13, 2019 (153)
112 ILLUMINA ss3745382570 Jul 13, 2019 (153)
113 EVA ss3765506371 Jul 13, 2019 (153)
114 PAGE_CC ss3771314779 Jul 13, 2019 (153)
115 ILLUMINA ss3772876003 Jul 13, 2019 (153)
116 ILLUMINA ss3772876004 Jul 13, 2019 (153)
117 PACBIO ss3785585322 Jul 13, 2019 (153)
118 PACBIO ss3790919451 Jul 13, 2019 (153)
119 PACBIO ss3795798649 Jul 13, 2019 (153)
120 KHV_HUMAN_GENOMES ss3808661264 Jul 13, 2019 (153)
121 EVA ss3830129040 Apr 26, 2020 (154)
122 EVA ss3838547908 Apr 26, 2020 (154)
123 EVA ss3843997105 Apr 26, 2020 (154)
124 HGDP ss3847846315 Apr 26, 2020 (154)
125 SGDP_PRJ ss3865426082 Apr 26, 2020 (154)
126 KRGDB ss3912352181 Apr 26, 2020 (154)
127 EVA ss3985244032 Apr 26, 2021 (155)
128 EVA ss4017293121 Apr 26, 2021 (155)
129 TOPMED ss4717100738 Apr 26, 2021 (155)
130 TOMMO_GENOMICS ss5179319453 Apr 26, 2021 (155)
131 EVA ss5237404927 Apr 26, 2021 (155)
132 1000G_HIGH_COVERAGE ss5269876989 Oct 13, 2022 (156)
133 EVA ss5315181674 Oct 13, 2022 (156)
134 EVA ss5368145889 Oct 13, 2022 (156)
135 HUGCELL_USP ss5467364110 Oct 13, 2022 (156)
136 EVA ss5508657259 Oct 13, 2022 (156)
137 1000G_HIGH_COVERAGE ss5556572824 Oct 13, 2022 (156)
138 SANFORD_IMAGENETICS ss5624638907 Oct 13, 2022 (156)
139 SANFORD_IMAGENETICS ss5641219840 Oct 13, 2022 (156)
140 TOMMO_GENOMICS ss5718035152 Oct 13, 2022 (156)
141 EVA ss5799698874 Oct 13, 2022 (156)
142 YY_MCH ss5807841493 Oct 13, 2022 (156)
143 EVA ss5842804333 Oct 13, 2022 (156)
144 EVA ss5847301344 Oct 13, 2022 (156)
145 EVA ss5848108965 Oct 13, 2022 (156)
146 EVA ss5855527538 Oct 13, 2022 (156)
147 EVA ss5885413467 Oct 13, 2022 (156)
148 EVA ss5969736675 Oct 13, 2022 (156)
149 EVA ss5979798280 Oct 13, 2022 (156)
150 1000Genomes NC_000006.11 - 109634828 Oct 12, 2018 (152)
151 1000Genomes_30x NC_000006.12 - 109313625 Oct 13, 2022 (156)
152 The Avon Longitudinal Study of Parents and Children NC_000006.11 - 109634828 Oct 12, 2018 (152)
153 Genetic variation in the Estonian population NC_000006.11 - 109634828 Oct 12, 2018 (152)
154 The Danish reference pan genome NC_000006.11 - 109634828 Apr 26, 2020 (154)
155 gnomAD - Genomes NC_000006.12 - 109313625 Apr 26, 2021 (155)
156 Genome of the Netherlands Release 5 NC_000006.11 - 109634828 Apr 26, 2020 (154)
157 HGDP-CEPH-db Supplement 1 NC_000006.10 - 109741521 Apr 26, 2020 (154)
158 HapMap NC_000006.12 - 109313625 Apr 26, 2020 (154)
159 KOREAN population from KRGDB NC_000006.11 - 109634828 Apr 26, 2020 (154)
160 Northern Sweden NC_000006.11 - 109634828 Jul 13, 2019 (153)
161 The PAGE Study NC_000006.12 - 109313625 Jul 13, 2019 (153)
162 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000006.11 - 109634828 Apr 26, 2021 (155)
163 Qatari NC_000006.11 - 109634828 Apr 26, 2020 (154)
164 SGDP_PRJ NC_000006.11 - 109634828 Apr 26, 2020 (154)
165 Siberian NC_000006.11 - 109634828 Apr 26, 2020 (154)
166 8.3KJPN NC_000006.11 - 109634828 Apr 26, 2021 (155)
167 14KJPN NC_000006.12 - 109313625 Oct 13, 2022 (156)
168 TopMed NC_000006.12 - 109313625 Apr 26, 2021 (155)
169 UK 10K study - Twins NC_000006.11 - 109634828 Oct 12, 2018 (152)
170 A Vietnamese Genetic Variation Database NC_000006.11 - 109634828 Jul 13, 2019 (153)
171 ALFA NC_000006.12 - 109313625 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)
rs59486160 May 25, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss77757665, ss3639325888, ss3639958248, ss3644002959 NC_000006.9:109741520:A:G NC_000006.12:109313624:A:G (self)
524207, ss93536546, ss110720000, ss114916354, ss160021710, ss162705031, ss164214024, ss207364284, ss254636733, ss278969393, ss293696756, ss479640050, ss1592920031, ss1712890264, ss3643589628, ss3847846315 NC_000006.10:109741520:A:G NC_000006.12:109313624:A:G (self)
33581894, 18710779, 13369606, 8007316, 8336503, 19529575, 7149383, 469959, 8648639, 17443062, 4663864, 37288760, 18710779, 4162514, ss222603565, ss233632003, ss240657129, ss479645309, ss480152680, ss484618700, ss491390146, ss536741803, ss559442012, ss653553139, ss778396277, ss780681256, ss782756167, ss783354560, ss783722710, ss832008364, ss832710466, ss833301155, ss833851396, ss983358557, ss1073927280, ss1321733469, ss1430856538, ss1581842377, ss1616408190, ss1659402223, ss1752594866, ss1752594867, ss1917809313, ss1926606709, ss1946187943, ss1946187944, ss1958940504, ss1958940505, ss2023952805, ss2152147510, ss2634495742, ss2634495743, ss2634495744, ss2707773906, ss2711086818, ss2843561107, ss2985377714, ss2986010302, ss2999735151, ss3022654685, ss3022654686, ss3347168903, ss3625909504, ss3629627005, ss3629627006, ss3632409964, ss3633433424, ss3634156848, ss3635082634, ss3635082635, ss3635837398, ss3636807421, ss3637590245, ss3638649999, ss3640789935, ss3640789936, ss3644921053, ss3644921054, ss3653174070, ss3653174071, ss3654144017, ss3667631358, ss3733864518, ss3744276788, ss3744558936, ss3745382569, ss3745382570, ss3765506371, ss3772876003, ss3772876004, ss3785585322, ss3790919451, ss3795798649, ss3830129040, ss3838547908, ss3865426082, ss3912352181, ss3985244032, ss4017293121, ss5179319453, ss5237404927, ss5315181674, ss5368145889, ss5508657259, ss5624638907, ss5641219840, ss5799698874, ss5842804333, ss5847301344, ss5848108965, ss5969736675, ss5979798280 NC_000006.11:109634827:A:G NC_000006.12:109313624:A:G (self)
44098759, 237127113, 3218643, 536248, 51872256, 554478296, 1004125774, ss2287242901, ss3025772208, ss3648443368, ss3718013709, ss3726373558, ss3771314779, ss3808661264, ss3843997105, ss4717100738, ss5269876989, ss5467364110, ss5556572824, ss5718035152, ss5807841493, ss5855527538, ss5885413467 NC_000006.12:109313624:A:G NC_000006.12:109313624:A:G (self)
ss17892962, ss22374558 NT_025741.13:13804256:A:G NC_000006.12:109313624:A:G (self)
ss42707515, ss66971634, ss67141122, ss68118054, ss70550251, ss71085471, ss75628959, ss85166486, ss98422827, ss143865867, ss153102975, ss157433399, ss159198003, ss171755965 NT_025741.15:13804284:A:G NC_000006.12:109313624:A:G (self)
Help

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

2 citations for rs11966072
PMID Title Author Year Journal
23446634 Genome-wide association analysis of red blood cell traits in African Americans: the COGENT Network. Chen Z et al. 2013 Human molecular genetics
29133146 Association of genetic polymorphisms with erythrocyte traits: Verification of SNPs reported in a previous GWAS in a Japanese population. Seiki T et al. 2018 Gene
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