Name: rs12022561
Published: September 21, 2022
License: Open Access

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.

rs12022561

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:79770134 (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: C=0.209283 (55395/264690, TOPMED)
C=0.196779 (51325/260826, ALFA)
C=0.198775 (40764/205076, GENOGRAPHIC) (+ 19 more)
C=0.27284 (21473/78702, PAGE_STUDY)
T=0.41089 (11610/28256, 14KJPN)
T=0.40901 (6855/16760, 8.3KJPN)
C=0.2692 (1724/6404, 1000G_30x)
C=0.2720 (1362/5008, 1000G)
C=0.2797 (1253/4480, Estonian)
C=0.1788 (689/3854, ALSPAC)
C=0.1764 (654/3708, TWINSUK)
T=0.3823 (1120/2930, KOREAN)
C=0.2585 (486/1880, HapMap)
T=0.3974 (728/1832, Korea1K)
C=0.179 (179/998, GoNL)
T=0.415 (313/754, PRJEB37584)
C=0.222 (133/600, NorthernSweden)
T=0.314 (93/296, SGDP_PRJ)
C=0.185 (40/216, Qatari)
C=0.407 (87/214, Vietnamese)
C=0.20 (8/40, GENOME_DK)
T=0.30 (12/40, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: None
Publications: 1 citation
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	261036	T=0.803261	C=0.196739, G=0.000000
European	Sub	222674	T=0.826446	C=0.173554, G=0.000000
African	Sub	6484	T=0.9237	C=0.0763, G=0.0000
African Others	Sub	260	T=0.923	C=0.077, G=0.000
African American	Sub	6224	T=0.9237	C=0.0763, G=0.0000
Asian	Sub	6718	T=0.4065	C=0.5935, G=0.0000
East Asian	Sub	4774	T=0.4016	C=0.5984, G=0.0000
Other Asian	Sub	1944	T=0.4187	C=0.5813, G=0.0000
Latin American 1	Sub	1102	T=0.8693	C=0.1307, G=0.0000
Latin American 2	Sub	8246	T=0.5212	C=0.4788, G=0.0000
South Asian	Sub	330	T=0.824	C=0.176, G=0.000
Other	Sub	15482	T=0.73660	C=0.26340, G=0.00000

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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	T=0.790717	C=0.209283
Allele Frequency Aggregator	Total	Global	260826	T=0.803221	C=0.196779, G=0.000000
Allele Frequency Aggregator	European	Sub	222500	T=0.826431	C=0.173569, G=0.000000
Allele Frequency Aggregator	Other	Sub	15460	T=0.73642	C=0.26358, G=0.00000
Allele Frequency Aggregator	Latin American 2	Sub	8246	T=0.5212	C=0.4788, G=0.0000
Allele Frequency Aggregator	Asian	Sub	6718	T=0.4065	C=0.5935, G=0.0000
Allele Frequency Aggregator	African	Sub	6470	T=0.9236	C=0.0764, G=0.0000
Allele Frequency Aggregator	Latin American 1	Sub	1102	T=0.8693	C=0.1307, G=0.0000
Allele Frequency Aggregator	South Asian	Sub	330	T=0.824	C=0.176, G=0.000
Genographic Project	Global	Study-wide	205076	T=0.801225	C=0.198775, G=0.000000
The PAGE Study	Global	Study-wide	78702	T=0.72716	C=0.27284
The PAGE Study	AfricanAmerican	Sub	32516	T=0.88381	C=0.11619
The PAGE Study	Mexican	Sub	10810	T=0.51582	C=0.48418
The PAGE Study	Asian	Sub	8318	T=0.4173	C=0.5827
The PAGE Study	PuertoRican	Sub	7918	T=0.7761	C=0.2239
The PAGE Study	NativeHawaiian	Sub	4534	T=0.5849	C=0.4151
The PAGE Study	Cuban	Sub	4230	T=0.8340	C=0.1660
The PAGE Study	Dominican	Sub	3828	T=0.8461	C=0.1539
The PAGE Study	CentralAmerican	Sub	2450	T=0.5208	C=0.4792
The PAGE Study	SouthAmerican	Sub	1982	T=0.5151	C=0.4849
The PAGE Study	NativeAmerican	Sub	1260	T=0.7317	C=0.2683
The PAGE Study	SouthAsian	Sub	856	T=0.772	C=0.228
14KJPN	JAPANESE	Study-wide	28256	T=0.41089	C=0.58911
8.3KJPN	JAPANESE	Study-wide	16760	T=0.40901	C=0.59099
1000Genomes_30x	Global	Study-wide	6404	T=0.7308	C=0.2692
1000Genomes_30x	African	Sub	1786	T=0.9104	C=0.0896
1000Genomes_30x	Europe	Sub	1266	T=0.8381	C=0.1619
1000Genomes_30x	South Asian	Sub	1202	T=0.7845	C=0.2155
1000Genomes_30x	East Asian	Sub	1170	T=0.4496	C=0.5504
1000Genomes_30x	American	Sub	980	T=0.535	C=0.465
1000Genomes	Global	Study-wide	5008	T=0.7280	C=0.2720
1000Genomes	African	Sub	1322	T=0.9100	C=0.0900
1000Genomes	East Asian	Sub	1008	T=0.4504	C=0.5496
1000Genomes	Europe	Sub	1006	T=0.8280	C=0.1720
1000Genomes	South Asian	Sub	978	T=0.793	C=0.207
1000Genomes	American	Sub	694	T=0.548	C=0.452
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.7203	C=0.2797
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.8212	C=0.1788
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.8236	C=0.1764
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.3823	C=0.6177
HapMap	Global	Study-wide	1880	T=0.7415	C=0.2585
HapMap	American	Sub	764	T=0.685	C=0.315
HapMap	African	Sub	690	T=0.900	C=0.100
HapMap	Asian	Sub	254	T=0.421	C=0.579
HapMap	Europe	Sub	172	T=0.831	C=0.169
Korean Genome Project	KOREAN	Study-wide	1832	T=0.3974	C=0.6026
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.821	C=0.179
CNV burdens in cranial meningiomas	Global	Study-wide	754	T=0.415	C=0.585
CNV burdens in cranial meningiomas	CRM	Sub	754	T=0.415	C=0.585
Northern Sweden	ACPOP	Study-wide	600	T=0.778	C=0.222
SGDP_PRJ	Global	Study-wide	296	T=0.314	C=0.686
Qatari	Global	Study-wide	216	T=0.815	C=0.185
A Vietnamese Genetic Variation Database	Global	Study-wide	214	T=0.593	C=0.407
The Danish reference pan genome	Danish	Study-wide	40	T=0.80	C=0.20
Siberian	Global	Study-wide	40	T=0.30	C=0.70

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 1	NC_000001.11:g.79770134T>C
GRCh38.p14 chr 1	NC_000001.11:g.79770134T>G
GRCh37.p13 chr 1	NC_000001.10:g.80235819T>C
GRCh37.p13 chr 1	NC_000001.10:g.80235819T>G

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

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 1	NC_000001.11:g.79770134=	NC_000001.11:g.79770134T>C	NC_000001.11:g.79770134T>G
GRCh37.p13 chr 1	NC_000001.10:g.80235819=	NC_000001.10:g.80235819T>C	NC_000001.10:g.80235819T>G

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#.

117 SubSNP, 24 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SC_SNP	ss18071702	Feb 28, 2004 (120)
2	ABI	ss41112081	Mar 13, 2006 (126)
3	PERLEGEN	ss46536130	Mar 13, 2006 (126)
4	AFFY	ss66036223	Jul 04, 2010 (132)
5	AFFY	ss75924935	Dec 08, 2007 (130)
6	KRIBB_YJKIM	ss82944453	Dec 15, 2007 (130)
7	HUMANGENOME_JCVI	ss97951193	Feb 02, 2009 (130)
8	BGI	ss102756030	Dec 01, 2009 (131)
9	1000GENOMES	ss108343830	Jan 23, 2009 (130)
10	ILLUMINA-UK	ss118834755	Feb 14, 2009 (130)
11	ENSEMBL	ss138886589	Dec 01, 2009 (131)
12	GMI	ss155235216	Dec 01, 2009 (131)
13	ILLUMINA	ss160026623	Dec 01, 2009 (131)
14	AFFY	ss169199720	Jul 04, 2010 (132)
15	BUSHMAN	ss198672125	Jul 04, 2010 (132)
16	BCM-HGSC-SUB	ss205273500	Jul 04, 2010 (132)
17	1000GENOMES	ss210567536	Jul 14, 2010 (132)
18	1000GENOMES	ss218477992	Jul 14, 2010 (132)
19	1000GENOMES	ss230602359	Jul 14, 2010 (132)
20	1000GENOMES	ss238282027	Jul 15, 2010 (132)
21	GMI	ss275892493	May 04, 2012 (137)
22	GMI	ss284080695	Apr 25, 2013 (138)
23	PJP	ss290545851	May 09, 2011 (134)
24	ILLUMINA	ss479653479	May 04, 2012 (137)
25	ILLUMINA	ss479658792	May 04, 2012 (137)
26	ILLUMINA	ss480172333	Sep 08, 2015 (146)
27	ILLUMINA	ss484625388	May 04, 2012 (137)
28	EXOME_CHIP	ss491295835	May 04, 2012 (137)
29	ILLUMINA	ss536747191	Sep 08, 2015 (146)
30	TISHKOFF	ss554299337	Apr 25, 2013 (138)
31	SSMP	ss648157768	Apr 25, 2013 (138)
32	ILLUMINA	ss778690785	Aug 21, 2014 (142)
33	ILLUMINA	ss780681280	Aug 21, 2014 (142)
34	ILLUMINA	ss782759508	Aug 21, 2014 (142)
35	ILLUMINA	ss783354584	Aug 21, 2014 (142)
36	ILLUMINA	ss783725978	Aug 21, 2014 (142)
37	ILLUMINA	ss832011745	Apr 01, 2015 (144)
38	ILLUMINA	ss834149514	Aug 21, 2014 (142)
39	EVA-GONL	ss975338135	Aug 21, 2014 (142)
40	JMKIDD_LAB	ss1068022847	Aug 21, 2014 (142)
41	1000GENOMES	ss1291571947	Aug 21, 2014 (142)
42	DDI	ss1425867445	Apr 01, 2015 (144)
43	EVA_GENOME_DK	ss1574175977	Apr 01, 2015 (144)
44	EVA_DECODE	ss1584711815	Apr 01, 2015 (144)
45	EVA_UK10K_ALSPAC	ss1600531796	Apr 01, 2015 (144)
46	EVA_UK10K_TWINSUK	ss1643525829	Apr 01, 2015 (144)
47	EVA_SVP	ss1712346441	Apr 01, 2015 (144)
48	ILLUMINA	ss1751934272	Sep 08, 2015 (146)
49	ILLUMINA	ss1751934273	Sep 08, 2015 (146)
50	HAMMER_LAB	ss1794614052	Sep 08, 2015 (146)
51	ILLUMINA	ss1917730484	Feb 12, 2016 (147)
52	WEILL_CORNELL_DGM	ss1918542585	Feb 12, 2016 (147)
53	ILLUMINA	ss1945999550	Feb 12, 2016 (147)
54	ILLUMINA	ss1958286591	Feb 12, 2016 (147)
55	GENOMED	ss1966787933	Jul 19, 2016 (147)
56	JJLAB	ss2019791463	Sep 14, 2016 (149)
57	USC_VALOUEV	ss2147807607	Dec 20, 2016 (150)
58	HUMAN_LONGEVITY	ss2163929789	Dec 20, 2016 (150)
59	SYSTEMSBIOZJU	ss2624406523	Nov 08, 2017 (151)
60	ILLUMINA	ss2632536752	Nov 08, 2017 (151)
61	GRF	ss2697728020	Nov 08, 2017 (151)
62	GNOMAD	ss2757091248	Nov 08, 2017 (151)
63	AFFY	ss2984865296	Nov 08, 2017 (151)
64	AFFY	ss2985517752	Nov 08, 2017 (151)
65	SWEGEN	ss2987085285	Nov 08, 2017 (151)
66	BIOINF_KMB_FNS_UNIBA	ss3023657823	Nov 08, 2017 (151)
67	CSHL	ss3343531763	Nov 08, 2017 (151)
68	ILLUMINA	ss3626135077	Oct 11, 2018 (152)
69	ILLUMINA	ss3626135078	Oct 11, 2018 (152)
70	ILLUMINA	ss3630571781	Oct 11, 2018 (152)
71	ILLUMINA	ss3632897784	Oct 11, 2018 (152)
72	ILLUMINA	ss3633592597	Oct 11, 2018 (152)
73	ILLUMINA	ss3634332483	Oct 11, 2018 (152)
74	ILLUMINA	ss3634332484	Oct 11, 2018 (152)
75	ILLUMINA	ss3635286328	Oct 11, 2018 (152)
76	ILLUMINA	ss3636009464	Oct 11, 2018 (152)
77	ILLUMINA	ss3637036770	Oct 11, 2018 (152)
78	ILLUMINA	ss3640039844	Oct 11, 2018 (152)
79	ILLUMINA	ss3640039845	Oct 11, 2018 (152)
80	ILLUMINA	ss3644495496	Oct 11, 2018 (152)
81	URBANLAB	ss3646700194	Oct 11, 2018 (152)
82	ILLUMINA	ss3653636825	Oct 11, 2018 (152)
83	EGCUT_WGS	ss3655164280	Jul 12, 2019 (153)
84	EVA_DECODE	ss3687103223	Jul 12, 2019 (153)
85	ACPOP	ss3727194885	Jul 12, 2019 (153)
86	ILLUMINA	ss3744347458	Jul 12, 2019 (153)
87	ILLUMINA	ss3744633456	Jul 12, 2019 (153)
88	ILLUMINA	ss3744633457	Jul 12, 2019 (153)
89	EVA	ss3746409659	Jul 12, 2019 (153)
90	PAGE_CC	ss3770819930	Jul 12, 2019 (153)
91	ILLUMINA	ss3772134754	Jul 12, 2019 (153)
92	ILLUMINA	ss3772134755	Jul 12, 2019 (153)
93	KHV_HUMAN_GENOMES	ss3799415590	Jul 12, 2019 (153)
94	EVA	ss3826258124	Apr 25, 2020 (154)
95	EVA	ss3836517510	Apr 25, 2020 (154)
96	EVA	ss3841924534	Apr 25, 2020 (154)
97	SGDP_PRJ	ss3849198410	Apr 25, 2020 (154)
98	KRGDB	ss3894246093	Apr 25, 2020 (154)
99	KOGIC	ss3944835753	Apr 25, 2020 (154)
100	EVA	ss3984459677	Apr 25, 2021 (155)
101	TOPMED	ss4455840485	Apr 25, 2021 (155)
102	TOMMO_GENOMICS	ss5144704354	Apr 25, 2021 (155)
103	1000G_HIGH_COVERAGE	ss5242855347	Oct 12, 2022 (156)
104	GENOGRAPHIC	ss5314465392	Oct 12, 2022 (156)
105	EVA	ss5314628009	Oct 12, 2022 (156)
106	EVA	ss5319817293	Oct 12, 2022 (156)
107	HUGCELL_USP	ss5443860721	Oct 12, 2022 (156)
108	EVA	ss5505913659	Oct 12, 2022 (156)
109	1000G_HIGH_COVERAGE	ss5515448205	Oct 12, 2022 (156)
110	SANFORD_IMAGENETICS	ss5625865831	Oct 12, 2022 (156)
111	TOMMO_GENOMICS	ss5669691839	Oct 12, 2022 (156)
112	EVA	ss5799489145	Oct 12, 2022 (156)
113	YY_MCH	ss5800741951	Oct 12, 2022 (156)
114	EVA	ss5832185401	Oct 12, 2022 (156)
115	EVA	ss5848977284	Oct 12, 2022 (156)
116	EVA	ss5908940389	Oct 12, 2022 (156)
117	EVA	ss5937712920	Oct 12, 2022 (156)
118	1000Genomes	NC_000001.10 - 80235819	Oct 11, 2018 (152)
119	1000Genomes_30x	NC_000001.11 - 79770134	Oct 12, 2022 (156)
120	The Avon Longitudinal Study of Parents and Children	NC_000001.10 - 80235819	Oct 11, 2018 (152)
121	Genetic variation in the Estonian population	NC_000001.10 - 80235819	Oct 11, 2018 (152)
122	Genographic Project	NC_000001.11 - 79770134	Oct 12, 2022 (156)
123	The Danish reference pan genome	NC_000001.10 - 80235819	Apr 25, 2020 (154)
124	gnomAD - Genomes Submission ignored due to conflicting rows: Row 16357924 (NC_000001.11:79770133:T:C 27765/140002) Row 16357925 (NC_000001.11:79770133:T:G 3/140048)	-	Apr 25, 2021 (155)
125	gnomAD - Genomes Submission ignored due to conflicting rows: Row 16357924 (NC_000001.11:79770133:T:C 27765/140002) Row 16357925 (NC_000001.11:79770133:T:G 3/140048)	-	Apr 25, 2021 (155)
126	Genome of the Netherlands Release 5	NC_000001.10 - 80235819	Apr 25, 2020 (154)
127	HapMap	NC_000001.11 - 79770134	Apr 25, 2020 (154)
128	KOREAN population from KRGDB	NC_000001.10 - 80235819	Apr 25, 2020 (154)
129	Korean Genome Project	NC_000001.11 - 79770134	Apr 25, 2020 (154)
130	Northern Sweden	NC_000001.10 - 80235819	Jul 12, 2019 (153)
131	The PAGE Study	NC_000001.11 - 79770134	Jul 12, 2019 (153)
132	CNV burdens in cranial meningiomas	NC_000001.10 - 80235819	Apr 25, 2021 (155)
133	Qatari	NC_000001.10 - 80235819	Apr 25, 2020 (154)
134	SGDP_PRJ	NC_000001.10 - 80235819	Apr 25, 2020 (154)
135	Siberian	NC_000001.10 - 80235819	Apr 25, 2020 (154)
136	8.3KJPN	NC_000001.10 - 80235819	Apr 25, 2021 (155)
137	14KJPN	NC_000001.11 - 79770134	Oct 12, 2022 (156)
138	TopMed	NC_000001.11 - 79770134	Apr 25, 2021 (155)
139	UK 10K study - Twins	NC_000001.10 - 80235819	Oct 11, 2018 (152)
140	A Vietnamese Genetic Variation Database	NC_000001.10 - 80235819	Jul 12, 2019 (153)
141	ALFA	NC_000001.11 - 79770134	Apr 25, 2021 (155)

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)
rs56554946	May 23, 2008 (130)
rs60181900	Feb 25, 2009 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss75924935, ss108343830, ss118834755, ss160026623, ss169199720, ss198672125, ss205273500, ss210567536, ss275892493, ss284080695, ss290545851, ss479653479, ss1584711815, ss1712346441	NC_000001.9:80008406:T:C	NC_000001.11:79770133:T:C	(self)
2315205, 1269750, 902528, 1572265, 545642, 1423487, 479750, 8987, 584515, 1215390, 323961, 2673661, 1269750, 269577, ss218477992, ss230602359, ss238282027, ss479658792, ss480172333, ss484625388, ss491295835, ss536747191, ss554299337, ss648157768, ss778690785, ss780681280, ss782759508, ss783354584, ss783725978, ss832011745, ss834149514, ss975338135, ss1068022847, ss1291571947, ss1425867445, ss1574175977, ss1600531796, ss1643525829, ss1751934272, ss1751934273, ss1794614052, ss1917730484, ss1918542585, ss1945999550, ss1958286591, ss1966787933, ss2019791463, ss2147807607, ss2624406523, ss2632536752, ss2697728020, ss2757091248, ss2984865296, ss2985517752, ss2987085285, ss3343531763, ss3626135077, ss3626135078, ss3630571781, ss3632897784, ss3633592597, ss3634332483, ss3634332484, ss3635286328, ss3636009464, ss3637036770, ss3640039844, ss3640039845, ss3644495496, ss3653636825, ss3655164280, ss3727194885, ss3744347458, ss3744633456, ss3744633457, ss3746409659, ss3772134754, ss3772134755, ss3826258124, ss3836517510, ss3849198410, ss3894246093, ss3984459677, ss5144704354, ss5314628009, ss5319817293, ss5505913659, ss5625865831, ss5799489145, ss5832185401, ss5937712920	NC_000001.10:80235818:T:C	NC_000001.11:79770133:T:C	(self)
2974140, 48756, 106908, 1213754, 41399, 3528943, 19446820, 14082050249, ss2163929789, ss3023657823, ss3646700194, ss3687103223, ss3770819930, ss3799415590, ss3841924534, ss3944835753, ss4455840485, ss5242855347, ss5314465392, ss5443860721, ss5515448205, ss5669691839, ss5800741951, ss5848977284, ss5908940389	NC_000001.11:79770133:T:C	NC_000001.11:79770133:T:C	(self)
ss18071702	NT_026943.13:5055992:T:C	NC_000001.11:79770133:T:C	(self)
ss41112081, ss46536130, ss82944453, ss97951193, ss102756030, ss138886589, ss155235216	NT_032977.9:50207736:T:C	NC_000001.11:79770133:T:C	(self)
ss66036223	NT_032977.10:79184145:T:C	NC_000001.11:79770133:T:C	(self)
ss2757091248	NC_000001.10:80235818:T:G	NC_000001.11:79770133:T:G	(self)
48756, 14082050249, ss2163929789, ss5314465392	NC_000001.11:79770133:T:G	NC_000001.11:79770133:T:G	(self)

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

1 citation for rs12022561

PMID	Title	Author	Year	Journal
31872004	Data on a genome-wide association study of type 2 diabetes in a Maya population.	Totomoch-Serra A et al.	2020	Data in brief

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.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs12022561