Name: rs12524967
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.

rs12524967

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:49619514 (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
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.260830 (69039/264690, TOPMED)
C=0.200898 (42944/213760, ALFA)
C=0.245014 (34325/140094, GnomAD) (+ 20 more)
C=0.43439 (12275/28258, 14KJPN)
C=0.43675 (7320/16760, 8.3KJPN)
C=0.2956 (1893/6404, 1000G_30x)
C=0.2941 (1473/5008, 1000G)
C=0.1752 (785/4480, Estonian)
C=0.1746 (673/3854, ALSPAC)
C=0.1888 (700/3708, TWINSUK)
C=0.4150 (1216/2930, KOREAN)
C=0.3340 (696/2084, HGDP_Stanford)
C=0.2858 (539/1886, HapMap)
C=0.2275 (258/1134, Daghestan)
C=0.198 (198/998, GoNL)
C=0.458 (287/626, Chileans)
C=0.163 (98/600, NorthernSweden)
T=0.359 (109/304, SGDP_PRJ)
C=0.273 (59/216, Qatari)
C=0.227 (49/216, Vietnamese)
C=0.08 (6/76, Ancient Sardinia)
C=0.15 (6/40, GENOME_DK)
T=0.41 (14/34, Siberian)

Clinical Significance: Reported in ClinVar
Gene : Consequence: RHAG : 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	213854	T=0.799120	C=0.200880
European	Sub	182602	T=0.820298	C=0.179702
African	Sub	7774	T=0.6861	C=0.3139
African Others	Sub	276	T=0.656	C=0.344
African American	Sub	7498	T=0.6872	C=0.3128
Asian	Sub	752	T=0.658	C=0.342
East Asian	Sub	574	T=0.664	C=0.336
Other Asian	Sub	178	T=0.640	C=0.360
Latin American 1	Sub	990	T=0.755	C=0.245
Latin American 2	Sub	9060	T=0.5440	C=0.4560
South Asian	Sub	5056	T=0.7623	C=0.2377
Other	Sub	7620	T=0.7543	C=0.2457

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=0.739170	C=0.260830
Allele Frequency Aggregator	Total	Global	213760	T=0.799102	C=0.200898
Allele Frequency Aggregator	European	Sub	182526	T=0.820289	C=0.179711
Allele Frequency Aggregator	Latin American 2	Sub	9060	T=0.5440	C=0.4560
Allele Frequency Aggregator	African	Sub	7774	T=0.6861	C=0.3139
Allele Frequency Aggregator	Other	Sub	7602	T=0.7541	C=0.2459
Allele Frequency Aggregator	South Asian	Sub	5056	T=0.7623	C=0.2377
Allele Frequency Aggregator	Latin American 1	Sub	990	T=0.755	C=0.245
Allele Frequency Aggregator	Asian	Sub	752	T=0.658	C=0.342
gnomAD - Genomes	Global	Study-wide	140094	T=0.754986	C=0.245014
gnomAD - Genomes	European	Sub	75886	T=0.81149	C=0.18851
gnomAD - Genomes	African	Sub	41988	T=0.69310	C=0.30690
gnomAD - Genomes	American	Sub	13634	T=0.62784	C=0.37216
gnomAD - Genomes	Ashkenazi Jewish	Sub	3322	T=0.8341	C=0.1659
gnomAD - Genomes	East Asian	Sub	3116	T=0.6871	C=0.3129
gnomAD - Genomes	Other	Sub	2148	T=0.7514	C=0.2486
14KJPN	JAPANESE	Study-wide	28258	T=0.56561	C=0.43439
8.3KJPN	JAPANESE	Study-wide	16760	T=0.56325	C=0.43675
1000Genomes_30x	Global	Study-wide	6404	T=0.7044	C=0.2956
1000Genomes_30x	African	Sub	1786	T=0.6758	C=0.3242
1000Genomes_30x	Europe	Sub	1266	T=0.8239	C=0.1761
1000Genomes_30x	South Asian	Sub	1202	T=0.7787	C=0.2213
1000Genomes_30x	East Asian	Sub	1170	T=0.6897	C=0.3103
1000Genomes_30x	American	Sub	980	T=0.529	C=0.471
1000Genomes	Global	Study-wide	5008	T=0.7059	C=0.2941
1000Genomes	African	Sub	1322	T=0.6785	C=0.3215
1000Genomes	East Asian	Sub	1008	T=0.6806	C=0.3194
1000Genomes	Europe	Sub	1006	T=0.8141	C=0.1859
1000Genomes	South Asian	Sub	978	T=0.780	C=0.220
1000Genomes	American	Sub	694	T=0.533	C=0.467
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.8248	C=0.1752
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.8254	C=0.1746
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.8112	C=0.1888
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.5850	C=0.4150
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	T=0.6660	C=0.3340
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	T=0.647	C=0.353
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	T=0.771	C=0.229
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	T=0.674	C=0.326
HGDP-CEPH-db Supplement 1	Europe	Sub	320	T=0.834	C=0.166
HGDP-CEPH-db Supplement 1	Africa	Sub	242	T=0.678	C=0.322
HGDP-CEPH-db Supplement 1	America	Sub	216	T=0.250	C=0.750
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	T=0.61	C=0.39
HapMap	Global	Study-wide	1886	T=0.7142	C=0.2858
HapMap	American	Sub	768	T=0.736	C=0.264
HapMap	African	Sub	688	T=0.711	C=0.289
HapMap	Asian	Sub	254	T=0.575	C=0.425
HapMap	Europe	Sub	176	T=0.835	C=0.165
Genome-wide autozygosity in Daghestan	Global	Study-wide	1134	T=0.7725	C=0.2275
Genome-wide autozygosity in Daghestan	Daghestan	Sub	626	T=0.807	C=0.193
Genome-wide autozygosity in Daghestan	Near_East	Sub	144	T=0.764	C=0.236
Genome-wide autozygosity in Daghestan	Central Asia	Sub	122	T=0.574	C=0.426
Genome-wide autozygosity in Daghestan	Europe	Sub	108	T=0.861	C=0.139
Genome-wide autozygosity in Daghestan	South Asian	Sub	98	T=0.71	C=0.29
Genome-wide autozygosity in Daghestan	Caucasus	Sub	36	T=0.78	C=0.22
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.802	C=0.198
Chileans	Chilean	Study-wide	626	T=0.542	C=0.458
Northern Sweden	ACPOP	Study-wide	600	T=0.837	C=0.163
SGDP_PRJ	Global	Study-wide	304	T=0.359	C=0.641
Qatari	Global	Study-wide	216	T=0.727	C=0.273
A Vietnamese Genetic Variation Database	Global	Study-wide	216	T=0.773	C=0.227
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	76	T=0.92	C=0.08
The Danish reference pan genome	Danish	Study-wide	40	T=0.85	C=0.15
Siberian	Global	Study-wide	34	T=0.41	C=0.59

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.49619514T>C
GRCh37.p13 chr 6	NC_000006.11:g.49587227T>C
RHAG RefSeqGene (LRG_822)	NG_011704.1:g.22361A>G

Gene: RHAG, Rh associated glycoprotein (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
RHAG transcript	NM_000324.3:c.158-152A>G	N/A	Intron Variant
RHAG transcript variant X1	XM_011514788.2:c.158-152A… XM_011514788.2:c.158-152A>G	N/A	Intron Variant

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.

Allele: C (allele ID: 1219771 )

ClinVar Accession	Disease Names	Clinical Significance
RCV001612152.3	not provided	Benign

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
GRCh38.p14 chr 6	NC_000006.12:g.49619514=	NC_000006.12:g.49619514T>C
GRCh37.p13 chr 6	NC_000006.11:g.49587227=	NC_000006.11:g.49587227T>C
RHAG RefSeqGene (LRG_822)	NG_011704.1:g.22361=	NG_011704.1:g.22361A>G
RHAG transcript	NM_000324.2:c.158-152=	NM_000324.2:c.158-152A>G
RHAG transcript	NM_000324.3:c.158-152=	NM_000324.3:c.158-152A>G
RHAG transcript variant X1	XM_011514788.2:c.158-152=	XM_011514788.2:c.158-152A>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#.

111 SubSNP, 23 Frequency, 1 ClinVar submissions

No	Submitter	Submission ID	Date (Build)
1	CSHL-HAPMAP	ss19659814	Feb 28, 2004 (120)
2	PERLEGEN	ss23943854	Sep 20, 2004 (123)
3	ABI	ss42851337	Mar 13, 2006 (126)
4	ILLUMINA	ss67016152	Nov 29, 2006 (127)
5	ILLUMINA	ss67336823	Nov 29, 2006 (127)
6	ILLUMINA	ss68131884	Dec 12, 2006 (127)
7	PERLEGEN	ss68976626	May 16, 2007 (127)
8	ILLUMINA	ss70572931	May 23, 2008 (130)
9	ILLUMINA	ss71113928	May 16, 2007 (127)
10	ILLUMINA	ss75924330	Dec 07, 2007 (129)
11	AFFY	ss76492008	Dec 08, 2007 (130)
12	KRIBB_YJKIM	ss85235607	Dec 14, 2007 (130)
13	ILLUMINA-UK	ss116459133	Feb 14, 2009 (130)
14	ILLUMINA	ss153222028	Dec 01, 2009 (131)
15	GMI	ss156911107	Dec 01, 2009 (131)
16	ILLUMINA	ss159222115	Dec 01, 2009 (131)
17	ILLUMINA	ss160279202	Dec 01, 2009 (131)
18	COMPLETE_GENOMICS	ss166648522	Jul 04, 2010 (132)
19	ILLUMINA	ss172136876	Jul 04, 2010 (132)
20	BUSHMAN	ss201804646	Jul 04, 2010 (132)
21	1000GENOMES	ss222386942	Jul 14, 2010 (132)
22	1000GENOMES	ss233467342	Jul 14, 2010 (132)
23	1000GENOMES	ss240525112	Jul 15, 2010 (132)
24	GMI	ss278790640	May 04, 2012 (137)
25	GMI	ss285401886	Apr 25, 2013 (138)
26	ILLUMINA	ss479763056	May 04, 2012 (137)
27	ILLUMINA	ss479769173	May 04, 2012 (137)
28	ILLUMINA	ss480333495	Sep 08, 2015 (146)
29	ILLUMINA	ss484679887	May 04, 2012 (137)
30	ILLUMINA	ss536790841	Sep 08, 2015 (146)
31	TISHKOFF	ss559198351	Apr 25, 2013 (138)
32	SSMP	ss653141124	Apr 25, 2013 (138)
33	ILLUMINA	ss780670047	Aug 21, 2014 (142)
34	ILLUMINA	ss782786771	Aug 21, 2014 (142)
35	ILLUMINA	ss783752586	Aug 21, 2014 (142)
36	ILLUMINA	ss832039441	Apr 01, 2015 (144)
37	ILLUMINA	ss832734490	Aug 21, 2014 (142)
38	ILLUMINA	ss833325320	Aug 21, 2014 (142)
39	ILLUMINA	ss836166012	Aug 21, 2014 (142)
40	EVA-GONL	ss982920736	Aug 21, 2014 (142)
41	JMKIDD_LAB	ss1073608575	Aug 21, 2014 (142)
42	1000GENOMES	ss1320090827	Aug 21, 2014 (142)
43	HAMMER_LAB	ss1397456140	Sep 08, 2015 (146)
44	DDI	ss1430718540	Apr 01, 2015 (144)
45	EVA_GENOME_DK	ss1581668594	Apr 01, 2015 (144)
46	EVA_DECODE	ss1592457451	Apr 01, 2015 (144)
47	EVA_UK10K_ALSPAC	ss1615559158	Apr 01, 2015 (144)
48	EVA_UK10K_TWINSUK	ss1658553191	Apr 01, 2015 (144)
49	EVA_SVP	ss1712862838	Apr 01, 2015 (144)
50	ILLUMINA	ss1752640377	Sep 08, 2015 (146)
51	HAMMER_LAB	ss1804424626	Sep 08, 2015 (146)
52	WEILL_CORNELL_DGM	ss1926177987	Feb 12, 2016 (147)
53	GENOMED	ss1970394109	Jul 19, 2016 (147)
54	JJLAB	ss2023728388	Sep 14, 2016 (149)
55	USC_VALOUEV	ss2151907309	Dec 20, 2016 (150)
56	HUMAN_LONGEVITY	ss2284001464	Dec 20, 2016 (150)
57	ILLUMINA	ss2634452220	Nov 08, 2017 (151)
58	GRF	ss2707507440	Nov 08, 2017 (151)
59	GNOMAD	ss2838884416	Nov 08, 2017 (151)
60	AFFY	ss2985369965	Nov 08, 2017 (151)
61	AFFY	ss2986000889	Nov 08, 2017 (151)
62	SWEGEN	ss2999045999	Nov 08, 2017 (151)
63	BIOINF_KMB_FNS_UNIBA	ss3025655875	Nov 08, 2017 (151)
64	CSHL	ss3346957227	Nov 08, 2017 (151)
65	ILLUMINA	ss3629547435	Oct 12, 2018 (152)
66	ILLUMINA	ss3632368908	Oct 12, 2018 (152)
67	ILLUMINA	ss3633421910	Oct 12, 2018 (152)
68	ILLUMINA	ss3634144834	Oct 12, 2018 (152)
69	ILLUMINA	ss3635068052	Oct 12, 2018 (152)
70	ILLUMINA	ss3635825661	Oct 12, 2018 (152)
71	ILLUMINA	ss3636790791	Oct 12, 2018 (152)
72	ILLUMINA	ss3637578479	Oct 12, 2018 (152)
73	ILLUMINA	ss3638630455	Oct 12, 2018 (152)
74	ILLUMINA	ss3639315670	Oct 12, 2018 (152)
75	ILLUMINA	ss3639953656	Oct 12, 2018 (152)
76	ILLUMINA	ss3640775352	Oct 12, 2018 (152)
77	ILLUMINA	ss3641195548	Oct 12, 2018 (152)
78	ILLUMINA	ss3641492708	Oct 12, 2018 (152)
79	ILLUMINA	ss3643571491	Oct 12, 2018 (152)
80	ILLUMINA	ss3643998603	Oct 12, 2018 (152)
81	ILLUMINA	ss3654135437	Oct 12, 2018 (152)
82	EGCUT_WGS	ss3666942467	Jul 13, 2019 (153)
83	EVA_DECODE	ss3717189610	Jul 13, 2019 (153)
84	ACPOP	ss3733495526	Jul 13, 2019 (153)
85	ILLUMINA	ss3745368008	Jul 13, 2019 (153)
86	EVA	ss3765009664	Jul 13, 2019 (153)
87	ILLUMINA	ss3772861536	Jul 13, 2019 (153)
88	KHV_HUMAN_GENOMES	ss3808155030	Jul 13, 2019 (153)
89	EVA	ss3829917936	Apr 26, 2020 (154)
90	HGDP	ss3847834008	Apr 26, 2020 (154)
91	SGDP_PRJ	ss3864560214	Apr 26, 2020 (154)
92	KRGDB	ss3911372859	Apr 26, 2020 (154)
93	EVA	ss3985223507	Apr 26, 2021 (155)
94	EVA	ss4017275231	Apr 26, 2021 (155)
95	TOPMED	ss4702623341	Apr 26, 2021 (155)
96	TOMMO_GENOMICS	ss5177457688	Apr 26, 2021 (155)
97	1000G_HIGH_COVERAGE	ss5268410262	Oct 13, 2022 (156)
98	EVA	ss5315156423	Oct 13, 2022 (156)
99	EVA	ss5365561596	Oct 13, 2022 (156)
100	HUGCELL_USP	ss5466086813	Oct 13, 2022 (156)
101	EVA	ss5508487825	Oct 13, 2022 (156)
102	1000G_HIGH_COVERAGE	ss5554288992	Oct 13, 2022 (156)
103	SANFORD_IMAGENETICS	ss5640380135	Oct 13, 2022 (156)
104	TOMMO_GENOMICS	ss5715490381	Oct 13, 2022 (156)
105	EVA	ss5799689091	Oct 13, 2022 (156)
106	YY_MCH	ss5807458421	Oct 13, 2022 (156)
107	EVA	ss5842228106	Oct 13, 2022 (156)
108	EVA	ss5855353780	Oct 13, 2022 (156)
109	EVA	ss5883776951	Oct 13, 2022 (156)
110	EVA	ss5968880703	Oct 13, 2022 (156)
111	EVA	ss5981236239	Oct 13, 2022 (156)
112	1000Genomes	NC_000006.11 - 49587227	Oct 12, 2018 (152)
113	1000Genomes_30x	NC_000006.12 - 49619514	Oct 13, 2022 (156)
114	The Avon Longitudinal Study of Parents and Children	NC_000006.11 - 49587227	Oct 12, 2018 (152)
115	Chileans	NC_000006.11 - 49587227	Apr 26, 2020 (154)
116	Genome-wide autozygosity in Daghestan	NC_000006.10 - 49695186	Apr 26, 2020 (154)
117	Genetic variation in the Estonian population	NC_000006.11 - 49587227	Oct 12, 2018 (152)
118	The Danish reference pan genome	NC_000006.11 - 49587227	Apr 26, 2020 (154)
119	gnomAD - Genomes	NC_000006.12 - 49619514	Apr 26, 2021 (155)
120	Genome of the Netherlands Release 5	NC_000006.11 - 49587227	Apr 26, 2020 (154)
121	HGDP-CEPH-db Supplement 1	NC_000006.10 - 49695186	Apr 26, 2020 (154)
122	HapMap	NC_000006.12 - 49619514	Apr 26, 2020 (154)
123	KOREAN population from KRGDB	NC_000006.11 - 49587227	Apr 26, 2020 (154)
124	Northern Sweden	NC_000006.11 - 49587227	Jul 13, 2019 (153)
125	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000006.11 - 49587227	Apr 26, 2021 (155)
126	Qatari	NC_000006.11 - 49587227	Apr 26, 2020 (154)
127	SGDP_PRJ	NC_000006.11 - 49587227	Apr 26, 2020 (154)
128	Siberian	NC_000006.11 - 49587227	Apr 26, 2020 (154)
129	8.3KJPN	NC_000006.11 - 49587227	Apr 26, 2021 (155)
130	14KJPN	NC_000006.12 - 49619514	Oct 13, 2022 (156)
131	TopMed	NC_000006.12 - 49619514	Apr 26, 2021 (155)
132	UK 10K study - Twins	NC_000006.11 - 49587227	Oct 12, 2018 (152)
133	A Vietnamese Genetic Variation Database	NC_000006.11 - 49587227	Jul 13, 2019 (153)
134	ALFA	NC_000006.12 - 49619514	Apr 26, 2021 (155)
135	ClinVar	RCV001612152.3	Oct 13, 2022 (156)

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)
rs56452721	May 23, 2008 (130)
rs57333713	May 23, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss3639315670, ss3639953656, ss3643998603	NC_000006.9:49695185:T:C	NC_000006.12:49619513:T:C	(self)
430760, 511900, ss76492008, ss116459133, ss160279202, ss166648522, ss201804646, ss278790640, ss285401886, ss479763056, ss1397456140, ss1592457451, ss1712862838, ss3643571491, ss3847834008	NC_000006.10:49695185:T:C	NC_000006.12:49619513:T:C	(self)
31877956, 17777491, 377921, 12680715, 7833533, 7910543, 18550253, 6780391, 449434, 8219917, 16577194, 4423663, 35426995, 17777491, 3945699, ss222386942, ss233467342, ss240525112, ss479769173, ss480333495, ss484679887, ss536790841, ss559198351, ss653141124, ss780670047, ss782786771, ss783752586, ss832039441, ss832734490, ss833325320, ss836166012, ss982920736, ss1073608575, ss1320090827, ss1430718540, ss1581668594, ss1615559158, ss1658553191, ss1752640377, ss1804424626, ss1926177987, ss1970394109, ss2023728388, ss2151907309, ss2634452220, ss2707507440, ss2838884416, ss2985369965, ss2986000889, ss2999045999, ss3346957227, ss3629547435, ss3632368908, ss3633421910, ss3634144834, ss3635068052, ss3635825661, ss3636790791, ss3637578479, ss3638630455, ss3640775352, ss3641195548, ss3641492708, ss3654135437, ss3666942467, ss3733495526, ss3745368008, ss3765009664, ss3772861536, ss3829917936, ss3864560214, ss3911372859, ss3985223507, ss4017275231, ss5177457688, ss5315156423, ss5365561596, ss5508487825, ss5640380135, ss5799689091, ss5842228106, ss5968880703, ss5981236239	NC_000006.11:49587226:T:C	NC_000006.12:49619513:T:C	(self)
RCV001612152.3, 41814927, 224899142, 3129923, 49327485, 540000899, 1957830623, ss2284001464, ss3025655875, ss3717189610, ss3808155030, ss4702623341, ss5268410262, ss5466086813, ss5554288992, ss5715490381, ss5807458421, ss5855353780, ss5883776951	NC_000006.12:49619513:T:C	NC_000006.12:49619513:T:C	(self)
ss19659814	NT_007592.13:40384334:T:C	NC_000006.12:49619513:T:C	(self)
ss23943854, ss42851337, ss67016152, ss67336823, ss68131884, ss68976626, ss70572931, ss71113928, ss75924330, ss85235607, ss153222028, ss156911107, ss159222115, ss172136876	NT_007592.15:49527226:T:C	NC_000006.12:49619513:T:C	(self)

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

No publications for rs12524967

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
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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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs12524967