Name: rs7488426
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.

rs7488426

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr12:9388200 (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>C / A>G / A>T
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.445925 (118032/264690, TOPMED)
A=0.498930 (119349/239210, ALFA)
C=0.453078 (63430/139998, GnomAD) (+ 19 more)
C=0.41772 (32702/78286, PAGE_STUDY)
C=0.46992 (13279/28258, 14KJPN)
C=0.47166 (7905/16760, 8.3KJPN)
C=0.4638 (2970/6404, 1000G_30x)
C=0.4704 (2356/5008, 1000G)
A=0.4998 (2239/4480, Estonian)
A=0.4896 (1887/3854, ALSPAC)
A=0.4938 (1831/3708, TWINSUK)
A=0.3949 (1157/2930, KOREAN)
A=0.4094 (750/1832, Korea1K)
C=0.3883 (483/1244, HapMap)
A=0.488 (487/998, GoNL)
A=0.405 (318/786, PRJEB37584)
C=0.447 (268/600, NorthernSweden)
A=0.343 (133/388, SGDP_PRJ)
A=0.440 (95/216, Qatari)
A=0.350 (75/214, Vietnamese)
A=0.34 (15/44, Siberian)
C=0.45 (18/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LINC02367 : 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	244244	A=0.499980	C=0.500020, T=0.000000
European	Sub	216644	A=0.491498	C=0.508502, T=0.000000
African	Sub	7910	A=0.7656	C=0.2344, T=0.0000
African Others	Sub	312	A=0.862	C=0.138, T=0.000
African American	Sub	7598	A=0.7616	C=0.2384, T=0.0000
Asian	Sub	3716	A=0.4440	C=0.5560, T=0.0000
East Asian	Sub	3010	A=0.4169	C=0.5831, T=0.0000
Other Asian	Sub	706	A=0.559	C=0.441, T=0.000
Latin American 1	Sub	906	A=0.571	C=0.429, T=0.000
Latin American 2	Sub	6040	A=0.4505	C=0.5495, T=0.0000
South Asian	Sub	302	A=0.583	C=0.417, T=0.000
Other	Sub	8726	A=0.5176	C=0.4824, T=0.0000

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	A=0.554075	C=0.445925
Allele Frequency Aggregator	Total	Global	239210	A=0.498930	C=0.501070, T=0.000000
Allele Frequency Aggregator	European	Sub	213552	A=0.491641	C=0.508359, T=0.000000
Allele Frequency Aggregator	Other	Sub	7926	A=0.5160	C=0.4840, T=0.0000
Allele Frequency Aggregator	African	Sub	6768	A=0.7689	C=0.2311, T=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	6040	A=0.4505	C=0.5495, T=0.0000
Allele Frequency Aggregator	Asian	Sub	3716	A=0.4440	C=0.5560, T=0.0000
Allele Frequency Aggregator	Latin American 1	Sub	906	A=0.571	C=0.429, T=0.000
Allele Frequency Aggregator	South Asian	Sub	302	A=0.583	C=0.417, T=0.000
gnomAD - Genomes	Global	Study-wide	139998	A=0.546922	C=0.453078
gnomAD - Genomes	European	Sub	75826	A=0.47985	C=0.52015
gnomAD - Genomes	African	Sub	41952	A=0.71401	C=0.28599
gnomAD - Genomes	American	Sub	13626	A=0.46984	C=0.53016
gnomAD - Genomes	Ashkenazi Jewish	Sub	3320	A=0.4611	C=0.5389
gnomAD - Genomes	East Asian	Sub	3130	A=0.3914	C=0.6086
gnomAD - Genomes	Other	Sub	2144	A=0.4995	C=0.5005
The PAGE Study	Global	Study-wide	78286	A=0.58228	C=0.41772
The PAGE Study	AfricanAmerican	Sub	32396	A=0.70814	C=0.29186
The PAGE Study	Mexican	Sub	10742	A=0.44210	C=0.55790
The PAGE Study	Asian	Sub	8256	A=0.5064	C=0.4936
The PAGE Study	PuertoRican	Sub	7884	A=0.5606	C=0.4394
The PAGE Study	NativeHawaiian	Sub	4482	A=0.4391	C=0.5609
The PAGE Study	Cuban	Sub	4210	A=0.5000	C=0.5000
The PAGE Study	Dominican	Sub	3808	A=0.5685	C=0.4315
The PAGE Study	CentralAmerican	Sub	2444	A=0.4709	C=0.5291
The PAGE Study	SouthAmerican	Sub	1970	A=0.4112	C=0.5888
The PAGE Study	NativeAmerican	Sub	1256	A=0.5000	C=0.5000
The PAGE Study	SouthAsian	Sub	838	A=0.556	C=0.444
14KJPN	JAPANESE	Study-wide	28258	A=0.53008	C=0.46992
8.3KJPN	JAPANESE	Study-wide	16760	A=0.52834	C=0.47166
1000Genomes_30x	Global	Study-wide	6404	A=0.5361	C=0.4638, T=0.0002
1000Genomes_30x	African	Sub	1786	A=0.7475	C=0.2525, T=0.0000
1000Genomes_30x	Europe	Sub	1266	A=0.4708	C=0.5292, T=0.0000
1000Genomes_30x	South Asian	Sub	1202	A=0.5283	C=0.4717, T=0.0000
1000Genomes_30x	East Asian	Sub	1170	A=0.3786	C=0.6205, T=0.0009
1000Genomes_30x	American	Sub	980	A=0.433	C=0.567, T=0.000
1000Genomes	Global	Study-wide	5008	A=0.5296	C=0.4704
1000Genomes	African	Sub	1322	A=0.7443	C=0.2557
1000Genomes	East Asian	Sub	1008	A=0.3859	C=0.6141
1000Genomes	Europe	Sub	1006	A=0.4563	C=0.5437
1000Genomes	South Asian	Sub	978	A=0.532	C=0.468
1000Genomes	American	Sub	694	A=0.432	C=0.568
Genetic variation in the Estonian population	Estonian	Study-wide	4480	A=0.4998	C=0.5002
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	A=0.4896	C=0.5104
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	A=0.4938	C=0.5062
KOREAN population from KRGDB	KOREAN	Study-wide	2930	A=0.3949	C=0.6051, G=0.0000
Korean Genome Project	KOREAN	Study-wide	1832	A=0.4094	C=0.5906
HapMap	Global	Study-wide	1244	A=0.6117	C=0.3883
HapMap	African	Sub	686	A=0.704	C=0.296
HapMap	American	Sub	392	A=0.495	C=0.505
HapMap	Asian	Sub	166	A=0.506	C=0.494
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	A=0.488	C=0.512
CNV burdens in cranial meningiomas	Global	Study-wide	786	A=0.405	C=0.595
CNV burdens in cranial meningiomas	CRM	Sub	786	A=0.405	C=0.595
Northern Sweden	ACPOP	Study-wide	600	A=0.553	C=0.447
SGDP_PRJ	Global	Study-wide	388	A=0.343	C=0.657
Qatari	Global	Study-wide	216	A=0.440	C=0.560
A Vietnamese Genetic Variation Database	Global	Study-wide	214	A=0.350	C=0.650
Siberian	Global	Study-wide	44	A=0.34	C=0.66
The Danish reference pan genome	Danish	Study-wide	40	A=0.55	C=0.45

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 12	NC_000012.12:g.9388200A>C
GRCh38.p14 chr 12	NC_000012.12:g.9388200A>G
GRCh38.p14 chr 12	NC_000012.12:g.9388200A>T
GRCh37.p13 chr 12	NC_000012.11:g.9540796A>C
GRCh37.p13 chr 12	NC_000012.11:g.9540796A>G
GRCh37.p13 chr 12	NC_000012.11:g.9540796A>T

Gene: LINC02367, long intergenic non-protein coding RNA 2367 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LINC02367 transcript	NR_120479.1:n.	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.

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	A=	C	G	T
GRCh38.p14 chr 12	NC_000012.12:g.9388200=	NC_000012.12:g.9388200A>C	NC_000012.12:g.9388200A>G	NC_000012.12:g.9388200A>T
GRCh37.p13 chr 12	NC_000012.11:g.9540796=	NC_000012.11:g.9540796A>C	NC_000012.11:g.9540796A>G	NC_000012.11:g.9540796A>T

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#.

115 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SC_JCM	ss11307074	Jul 11, 2003 (116)
2	SC_SNP	ss15645862	Feb 27, 2004 (120)
3	CSHL-HAPMAP	ss16589076	Feb 27, 2004 (120)
4	ILLUMINA	ss75269281	Dec 07, 2007 (129)
5	HGSV	ss84762814	Dec 15, 2007 (130)
6	BCMHGSC_JDW	ss88955868	Mar 24, 2008 (129)
7	HUMANGENOME_JCVI	ss97284954	Feb 05, 2009 (130)
8	BGI	ss103022637	Feb 23, 2009 (135)
9	1000GENOMES	ss111458739	Jan 25, 2009 (130)
10	1000GENOMES	ss113147894	Jan 25, 2009 (130)
11	KRIBB_YJKIM	ss119554980	Dec 01, 2009 (131)
12	ENSEMBL	ss132990368	Dec 01, 2009 (131)
13	ENSEMBL	ss137350413	Dec 01, 2009 (131)
14	GMI	ss157089109	Dec 01, 2009 (131)
15	ILLUMINA	ss160881683	Dec 01, 2009 (131)
16	COMPLETE_GENOMICS	ss167759602	Jul 04, 2010 (132)
17	COMPLETE_GENOMICS	ss169024027	Jul 04, 2010 (132)
18	COMPLETE_GENOMICS	ss170370726	Jul 04, 2010 (132)
19	ILLUMINA	ss174383517	Jul 04, 2010 (132)
20	BUSHMAN	ss203529863	Jul 04, 2010 (132)
21	1000GENOMES	ss225598460	Jul 14, 2010 (132)
22	1000GENOMES	ss235817298	Jul 15, 2010 (132)
23	1000GENOMES	ss242397261	Jul 15, 2010 (132)
24	GMI	ss281268165	May 04, 2012 (137)
25	PJP	ss291320383	May 09, 2011 (134)
26	ILLUMINA	ss481572576	May 04, 2012 (137)
27	ILLUMINA	ss481602417	May 04, 2012 (137)
28	ILLUMINA	ss482574043	Sep 08, 2015 (146)
29	ILLUMINA	ss485581338	May 04, 2012 (137)
30	ILLUMINA	ss537474327	Sep 08, 2015 (146)
31	TISHKOFF	ss562984954	Apr 25, 2013 (138)
32	SSMP	ss658514789	Apr 25, 2013 (138)
33	ILLUMINA	ss778603921	Aug 21, 2014 (142)
34	ILLUMINA	ss783236240	Aug 21, 2014 (142)
35	ILLUMINA	ss784190230	Aug 21, 2014 (142)
36	ILLUMINA	ss832496747	Apr 01, 2015 (144)
37	ILLUMINA	ss834061240	Aug 21, 2014 (142)
38	EVA-GONL	ss989224293	Aug 21, 2014 (142)
39	JMKIDD_LAB	ss1078236852	Aug 21, 2014 (142)
40	1000GENOMES	ss1388103116	Apr 01, 2015 (144)
41	DDI	ss1426838779	Apr 01, 2015 (144)
42	EVA_GENOME_DK	ss1576105014	Apr 01, 2015 (144)
43	EVA_DECODE	ss1598894383	Apr 01, 2015 (144)
44	EVA_UK10K_ALSPAC	ss1627989304	Apr 01, 2015 (144)
45	EVA_UK10K_TWINSUK	ss1670983337	Apr 01, 2015 (144)
46	EVA_SVP	ss1713305850	Apr 01, 2015 (144)
47	ILLUMINA	ss1752087081	Sep 08, 2015 (146)
48	WEILL_CORNELL_DGM	ss1932588450	Feb 12, 2016 (147)
49	ILLUMINA	ss1946331136	Feb 12, 2016 (147)
50	ILLUMINA	ss1959412111	Feb 12, 2016 (147)
51	GENOMED	ss1967518854	Jul 19, 2016 (147)
52	JJLAB	ss2027039306	Sep 14, 2016 (149)
53	USC_VALOUEV	ss2155361318	Dec 20, 2016 (150)
54	HUMAN_LONGEVITY	ss2187689331	Dec 20, 2016 (150)
55	SYSTEMSBIOZJU	ss2627997763	Nov 08, 2017 (151)
56	ILLUMINA	ss2632923337	Nov 08, 2017 (151)
57	GRF	ss2699685310	Nov 08, 2017 (151)
58	ILLUMINA	ss2710753776	Nov 08, 2017 (151)
59	GNOMAD	ss2907200180	Nov 08, 2017 (151)
60	SWEGEN	ss3009182651	Nov 08, 2017 (151)
61	ILLUMINA	ss3021404759	Nov 08, 2017 (151)
62	BIOINF_KMB_FNS_UNIBA	ss3027323661	Nov 08, 2017 (151)
63	CSHL	ss3349916045	Nov 08, 2017 (151)
64	ILLUMINA	ss3625615627	Oct 12, 2018 (152)
65	ILLUMINA	ss3626813119	Oct 12, 2018 (152)
66	ILLUMINA	ss3630935102	Oct 12, 2018 (152)
67	ILLUMINA	ss3633009733	Oct 12, 2018 (152)
68	ILLUMINA	ss3633710223	Oct 12, 2018 (152)
69	ILLUMINA	ss3634490336	Oct 12, 2018 (152)
70	ILLUMINA	ss3635401267	Oct 12, 2018 (152)
71	ILLUMINA	ss3636174341	Oct 12, 2018 (152)
72	ILLUMINA	ss3637152221	Oct 12, 2018 (152)
73	ILLUMINA	ss3637946397	Oct 12, 2018 (152)
74	ILLUMINA	ss3640197669	Oct 12, 2018 (152)
75	ILLUMINA	ss3642941390	Oct 12, 2018 (152)
76	ILLUMINA	ss3644584086	Oct 12, 2018 (152)
77	URBANLAB	ss3649761585	Oct 12, 2018 (152)
78	ILLUMINA	ss3651777223	Oct 12, 2018 (152)
79	EGCUT_WGS	ss3676505186	Jul 13, 2019 (153)
80	EVA_DECODE	ss3693088391	Jul 13, 2019 (153)
81	ILLUMINA	ss3725302063	Jul 13, 2019 (153)
82	ACPOP	ss3738758484	Jul 13, 2019 (153)
83	ILLUMINA	ss3744094875	Jul 13, 2019 (153)
84	ILLUMINA	ss3744791051	Jul 13, 2019 (153)
85	EVA	ss3750124791	Jul 13, 2019 (153)
86	PAGE_CC	ss3771673722	Jul 13, 2019 (153)
87	ILLUMINA	ss3772290618	Jul 13, 2019 (153)
88	KHV_HUMAN_GENOMES	ss3815441170	Jul 13, 2019 (153)
89	EVA	ss3832967501	Apr 26, 2020 (154)
90	EVA	ss3840048319	Apr 26, 2020 (154)
91	EVA	ss3845531245	Apr 26, 2020 (154)
92	SGDP_PRJ	ss3877662784	Apr 26, 2020 (154)
93	KRGDB	ss3926170690	Apr 26, 2020 (154)
94	KOGIC	ss3971259673	Apr 26, 2020 (154)
95	EVA	ss3984662135	Apr 26, 2021 (155)
96	EVA	ss4017573367	Apr 26, 2021 (155)
97	TOPMED	ss4908253152	Apr 26, 2021 (155)
98	TOMMO_GENOMICS	ss5205005806	Apr 26, 2021 (155)
99	1000G_HIGH_COVERAGE	ss5289763462	Oct 13, 2022 (156)
100	EVA	ss5315599431	Oct 13, 2022 (156)
101	EVA	ss5403840071	Oct 13, 2022 (156)
102	HUGCELL_USP	ss5484655391	Oct 13, 2022 (156)
103	EVA	ss5510590980	Oct 13, 2022 (156)
104	1000G_HIGH_COVERAGE	ss5586663853	Oct 13, 2022 (156)
105	SANFORD_IMAGENETICS	ss5624294242	Oct 13, 2022 (156)
106	SANFORD_IMAGENETICS	ss5652566703	Oct 13, 2022 (156)
107	TOMMO_GENOMICS	ss5753783697	Oct 13, 2022 (156)
108	EVA	ss5799863356	Oct 13, 2022 (156)
109	YY_MCH	ss5812996279	Oct 13, 2022 (156)
110	EVA	ss5837570691	Oct 13, 2022 (156)
111	EVA	ss5847404032	Oct 13, 2022 (156)
112	EVA	ss5850254418	Oct 13, 2022 (156)
113	EVA	ss5903235654	Oct 13, 2022 (156)
114	EVA	ss5943913081	Oct 13, 2022 (156)
115	EVA	ss5979382061	Oct 13, 2022 (156)
116	1000Genomes	NC_000012.11 - 9540796	Oct 12, 2018 (152)
117	1000Genomes_30x	NC_000012.12 - 9388200	Oct 13, 2022 (156)
118	The Avon Longitudinal Study of Parents and Children	NC_000012.11 - 9540796	Oct 12, 2018 (152)
119	Genetic variation in the Estonian population	NC_000012.11 - 9540796	Oct 12, 2018 (152)
120	The Danish reference pan genome	NC_000012.11 - 9540796	Apr 26, 2020 (154)
121	gnomAD - Genomes	NC_000012.12 - 9388200	Apr 26, 2021 (155)
122	Genome of the Netherlands Release 5	NC_000012.11 - 9540796	Apr 26, 2020 (154)
123	HapMap	NC_000012.12 - 9388200	Apr 26, 2020 (154)
124	KOREAN population from KRGDB	NC_000012.11 - 9540796	Apr 26, 2020 (154)
125	Korean Genome Project	NC_000012.12 - 9388200	Apr 26, 2020 (154)
126	Northern Sweden	NC_000012.11 - 9540796	Jul 13, 2019 (153)
127	The PAGE Study	NC_000012.12 - 9388200	Jul 13, 2019 (153)
128	CNV burdens in cranial meningiomas	NC_000012.11 - 9540796	Apr 26, 2021 (155)
129	Qatari	NC_000012.11 - 9540796	Apr 26, 2020 (154)
130	SGDP_PRJ	NC_000012.11 - 9540796	Apr 26, 2020 (154)
131	Siberian	NC_000012.11 - 9540796	Apr 26, 2020 (154)
132	8.3KJPN	NC_000012.11 - 9540796	Apr 26, 2021 (155)
133	14KJPN	NC_000012.12 - 9388200	Oct 13, 2022 (156)
134	TopMed	NC_000012.12 - 9388200	Apr 26, 2021 (155)
135	UK 10K study - Twins	NC_000012.11 - 9540796	Oct 12, 2018 (152)
136	A Vietnamese Genetic Variation Database	NC_000012.11 - 9540796	Jul 13, 2019 (153)
137	ALFA	NC_000012.12 - 9388200	Apr 26, 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)
rs59969738	May 25, 2008 (130)
rs74240355	Sep 17, 2011 (135)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss84762814	NC_000012.9:9432062:A:C	NC_000012.12:9388199:A:C	(self)
ss88955868, ss111458739, ss113147894, ss160881683, ss167759602, ss169024027, ss170370726, ss203529863, ss281268165, ss291320383, ss481572576, ss1598894383, ss1713305850, ss3642941390	NC_000012.10:9432062:A:C	NC_000012.12:9388199:A:C	(self)
56569764, 31411026, 22243434, 2837576, 14013454, 33348084, 12043349, 211626, 14630380, 29679764, 7877672, 62975113, 31411026, 6967429, ss225598460, ss235817298, ss242397261, ss481602417, ss482574043, ss485581338, ss537474327, ss562984954, ss658514789, ss778603921, ss783236240, ss784190230, ss832496747, ss834061240, ss989224293, ss1078236852, ss1388103116, ss1426838779, ss1576105014, ss1627989304, ss1670983337, ss1752087081, ss1932588450, ss1946331136, ss1959412111, ss1967518854, ss2027039306, ss2155361318, ss2627997763, ss2632923337, ss2699685310, ss2710753776, ss2907200180, ss3009182651, ss3021404759, ss3349916045, ss3625615627, ss3626813119, ss3630935102, ss3633009733, ss3633710223, ss3634490336, ss3635401267, ss3636174341, ss3637152221, ss3637946397, ss3640197669, ss3644584086, ss3651777223, ss3676505186, ss3738758484, ss3744094875, ss3744791051, ss3750124791, ss3772290618, ss3832967501, ss3840048319, ss3877662784, ss3926170690, ss3984662135, ss4017573367, ss5205005806, ss5315599431, ss5403840071, ss5510590980, ss5624294242, ss5652566703, ss5799863356, ss5837570691, ss5847404032, ss5943913081, ss5979382061	NC_000012.11:9540795:A:C	NC_000012.12:9388199:A:C	(self)
74189788, 398901442, 752710, 27637674, 895191, 87620801, 123798809, 12872729940, ss2187689331, ss3027323661, ss3649761585, ss3693088391, ss3725302063, ss3771673722, ss3815441170, ss3845531245, ss3971259673, ss4908253152, ss5289763462, ss5484655391, ss5586663853, ss5753783697, ss5812996279, ss5850254418, ss5903235654	NC_000012.12:9388199:A:C	NC_000012.12:9388199:A:C	(self)
ss11307074	NT_009714.15:2299769:A:C	NC_000012.12:9388199:A:C	(self)
ss15645862, ss16589076	NT_009714.16:2299769:A:C	NC_000012.12:9388199:A:C	(self)
ss75269281, ss97284954, ss103022637, ss119554980, ss132990368, ss137350413, ss157089109, ss174383517	NT_009714.17:2300919:A:C	NC_000012.12:9388199:A:C	(self)
33348084, ss3926170690	NC_000012.11:9540795:A:G	NC_000012.12:9388199:A:G	(self)
74189788, 12872729940, ss5586663853	NC_000012.12:9388199:A:T	NC_000012.12:9388199:A:T	(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 rs7488426

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

rs7488426