Name: rs56229264
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.

rs56229264

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr8:27463672 (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: G>A
Variation Type: SNV Single Nucleotide Variation
Frequency: A=0.012127 (3210/264690, TOPMED)
A=0.014285 (3592/251444, GnomAD_exome)
A=0.012567 (1762/140206, GnomAD) (+ 17 more)
A=0.013947 (1693/121390, ExAC)
A=0.01986 (1683/84762, ALFA)
A=0.01338 (174/13006, GO-ESP)
A=0.0058 (37/6404, 1000G_30x)
A=0.0060 (30/5008, 1000G)
A=0.0237 (106/4480, Estonian)
A=0.0158 (61/3854, ALSPAC)
A=0.0143 (53/3708, TWINSUK)
A=0.021 (21/998, GoNL)
A=0.022 (13/600, NorthernSweden)
A=0.030 (16/534, MGP)
A=0.010 (3/304, FINRISK)
A=0.019 (4/216, Qatari)
G=0.5 (4/8, SGDP_PRJ)
A=0.5 (4/8, SGDP_PRJ)
G=0.5 (3/6, Siberian)
A=0.5 (3/6, Siberian)

Clinical Significance: Reported in ClinVar
Gene : Consequence: CHRNA2 : Synonymous 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	101218	G=0.981061	A=0.018939
European	Sub	82158	G=0.97928	A=0.02072
African	Sub	8468	G=0.9962	A=0.0038
African Others	Sub	308	G=1.000	A=0.000
African American	Sub	8160	G=0.9961	A=0.0039
Asian	Sub	168	G=1.000	A=0.000
East Asian	Sub	112	G=1.000	A=0.000
Other Asian	Sub	56	G=1.00	A=0.00
Latin American 1	Sub	500	G=0.994	A=0.006
Latin American 2	Sub	648	G=0.989	A=0.011
South Asian	Sub	98	G=0.99	A=0.01
Other	Sub	9178	G=0.9813	A=0.0187

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	G=0.987873	A=0.012127
gnomAD - Exomes	Global	Study-wide	251444	G=0.985715	A=0.014285
gnomAD - Exomes	European	Sub	135372	G=0.980698	A=0.019302
gnomAD - Exomes	Asian	Sub	49010	G=0.99484	A=0.00516
gnomAD - Exomes	American	Sub	34592	G=0.98904	A=0.01096
gnomAD - Exomes	African	Sub	16256	G=0.99711	A=0.00289
gnomAD - Exomes	Ashkenazi Jewish	Sub	10078	G=0.98125	A=0.01875
gnomAD - Exomes	Other	Sub	6136	G=0.9819	A=0.0181
gnomAD - Genomes	Global	Study-wide	140206	G=0.987433	A=0.012567
gnomAD - Genomes	European	Sub	75938	G=0.98154	A=0.01846
gnomAD - Genomes	African	Sub	42018	G=0.99710	A=0.00290
gnomAD - Genomes	American	Sub	13650	G=0.99011	A=0.00989
gnomAD - Genomes	Ashkenazi Jewish	Sub	3320	G=0.9777	A=0.0223
gnomAD - Genomes	East Asian	Sub	3130	G=1.0000	A=0.0000
gnomAD - Genomes	Other	Sub	2150	G=0.9865	A=0.0135
ExAC	Global	Study-wide	121390	G=0.986053	A=0.013947
ExAC	Europe	Sub	73334	G=0.98070	A=0.01930
ExAC	Asian	Sub	25166	G=0.99483	A=0.00517
ExAC	American	Sub	11578	G=0.99093	A=0.00907
ExAC	African	Sub	10406	G=0.99683	A=0.00317
ExAC	Other	Sub	906	G=0.989	A=0.011
Allele Frequency Aggregator	Total	Global	84762	G=0.98014	A=0.01986
Allele Frequency Aggregator	European	Sub	71992	G=0.97896	A=0.02104
Allele Frequency Aggregator	Other	Sub	7726	G=0.9823	A=0.0177
Allele Frequency Aggregator	African	Sub	3630	G=0.9945	A=0.0055
Allele Frequency Aggregator	Latin American 2	Sub	648	G=0.989	A=0.011
Allele Frequency Aggregator	Latin American 1	Sub	500	G=0.994	A=0.006
Allele Frequency Aggregator	Asian	Sub	168	G=1.000	A=0.000
Allele Frequency Aggregator	South Asian	Sub	98	G=0.99	A=0.01
GO Exome Sequencing Project	Global	Study-wide	13006	G=0.98662	A=0.01338
GO Exome Sequencing Project	European American	Sub	8600	G=0.9817	A=0.0183
GO Exome Sequencing Project	African American	Sub	4406	G=0.9961	A=0.0039
1000Genomes_30x	Global	Study-wide	6404	G=0.9942	A=0.0058
1000Genomes_30x	African	Sub	1786	G=0.9994	A=0.0006
1000Genomes_30x	Europe	Sub	1266	G=0.9858	A=0.0142
1000Genomes_30x	South Asian	Sub	1202	G=0.9933	A=0.0067
1000Genomes_30x	East Asian	Sub	1170	G=1.0000	A=0.0000
1000Genomes_30x	American	Sub	980	G=0.990	A=0.010
1000Genomes	Global	Study-wide	5008	G=0.9940	A=0.0060
1000Genomes	African	Sub	1322	G=0.9992	A=0.0008
1000Genomes	East Asian	Sub	1008	G=1.0000	A=0.0000
1000Genomes	Europe	Sub	1006	G=0.9841	A=0.0159
1000Genomes	South Asian	Sub	978	G=0.995	A=0.005
1000Genomes	American	Sub	694	G=0.988	A=0.012
Genetic variation in the Estonian population	Estonian	Study-wide	4480	G=0.9763	A=0.0237
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	G=0.9842	A=0.0158
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	G=0.9857	A=0.0143
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	G=0.979	A=0.021
Northern Sweden	ACPOP	Study-wide	600	G=0.978	A=0.022
Medical Genome Project healthy controls from Spanish population	Spanish controls	Study-wide	534	G=0.970	A=0.030
FINRISK	Finnish from FINRISK project	Study-wide	304	G=0.990	A=0.010
Qatari	Global	Study-wide	216	G=0.981	A=0.019
SGDP_PRJ	Global	Study-wide	8	G=0.5	A=0.5
Siberian	Global	Study-wide	6	G=0.5	A=0.5

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 8	NC_000008.11:g.27463672G>A
GRCh37.p13 chr 8	NC_000008.10:g.27321189G>A
CHRNA2 RefSeqGene	NG_015827.1:g.20625C>T

Gene: CHRNA2, cholinergic receptor nicotinic alpha 2 subunit (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CHRNA2 transcript variant 1	NM_000742.4:c.771C>T	Y [TAC] > Y [TAT]	Coding Sequence Variant
neuronal acetylcholine receptor subunit alpha-2 isoform 1 precursor	NP_000733.2:p.Tyr257=	Y (Tyr) > Y (Tyr)	Synonymous Variant
CHRNA2 transcript variant 3	NM_001347705.2:c.294C>T	Y [TAC] > Y [TAT]	Coding Sequence Variant
neuronal acetylcholine receptor subunit alpha-2 isoform 3	NP_001334634.1:p.Tyr98=	Y (Tyr) > Y (Tyr)	Synonymous Variant
CHRNA2 transcript variant 6	NM_001347708.2:c.177C>T	Y [TAC] > Y [TAT]	Coding Sequence Variant
neuronal acetylcholine receptor subunit alpha-2 isoform 4	NP_001334637.1:p.Tyr59=	Y (Tyr) > Y (Tyr)	Synonymous Variant
CHRNA2 transcript variant 5	NM_001347707.2:c.177C>T	Y [TAC] > Y [TAT]	Coding Sequence Variant
neuronal acetylcholine receptor subunit alpha-2 isoform 4	NP_001334636.1:p.Tyr59=	Y (Tyr) > Y (Tyr)	Synonymous Variant
CHRNA2 transcript variant 4	NM_001347706.2:c.294C>T	Y [TAC] > Y [TAT]	Coding Sequence Variant
neuronal acetylcholine receptor subunit alpha-2 isoform 3	NP_001334635.1:p.Tyr98=	Y (Tyr) > Y (Tyr)	Synonymous Variant
CHRNA2 transcript variant 2	NM_001282455.2:c.726C>T	Y [TAC] > Y [TAT]	Coding Sequence Variant
neuronal acetylcholine receptor subunit alpha-2 isoform 2 precursor	NP_001269384.1:p.Tyr242=	Y (Tyr) > Y (Tyr)	Synonymous Variant
CHRNA2 transcript variant X1	XM_047421311.1:c.771C>T	Y [TAC] > Y [TAT]	Coding Sequence Variant
neuronal acetylcholine receptor subunit alpha-2 isoform X1	XP_047277267.1:p.Tyr257=	Y (Tyr) > Y (Tyr)	Synonymous Variant
CHRNA2 transcript variant X2	XM_047421312.1:c.771C>T	Y [TAC] > Y [TAT]	Coding Sequence Variant
neuronal acetylcholine receptor subunit alpha-2 isoform X1	XP_047277268.1:p.Tyr257=	Y (Tyr) > Y (Tyr)	Synonymous Variant
CHRNA2 transcript variant X3	XM_047421313.1:c.771C>T	Y [TAC] > Y [TAT]	Coding Sequence Variant
neuronal acetylcholine receptor subunit alpha-2 isoform X1	XP_047277269.1:p.Tyr257=	Y (Tyr) > Y (Tyr)	Synonymous 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: A (allele ID: 134190 )

ClinVar Accession	Disease Names	Clinical Significance
RCV000116714.6	not specified	Likely-Benign
RCV000369041.4	Autosomal dominant nocturnal frontal lobe epilepsy 4	Benign
RCV000460445.7	Autosomal dominant nocturnal frontal lobe epilepsy	Benign
RCV000716400.2	Seizure	Benign
RCV001668226.3	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	G=	A
GRCh38.p14 chr 8	NC_000008.11:g.27463672=	NC_000008.11:g.27463672G>A
GRCh37.p13 chr 8	NC_000008.10:g.27321189=	NC_000008.10:g.27321189G>A
CHRNA2 RefSeqGene	NG_015827.1:g.20625=	NG_015827.1:g.20625C>T
CHRNA2 transcript variant 1	NM_000742.4:c.771=	NM_000742.4:c.771C>T
CHRNA2 transcript variant 1	NM_000742.3:c.771=	NM_000742.3:c.771C>T
CHRNA2 transcript variant 4	NM_001347706.2:c.294=	NM_001347706.2:c.294C>T
CHRNA2 transcript variant 4	NM_001347706.1:c.294=	NM_001347706.1:c.294C>T
CHRNA2 transcript variant 2	NM_001282455.2:c.726=	NM_001282455.2:c.726C>T
CHRNA2 transcript variant 2	NM_001282455.1:c.726=	NM_001282455.1:c.726C>T
CHRNA2 transcript variant 3	NM_001347705.2:c.294=	NM_001347705.2:c.294C>T
CHRNA2 transcript variant 3	NM_001347705.1:c.294=	NM_001347705.1:c.294C>T
CHRNA2 transcript variant 5	NM_001347707.2:c.177=	NM_001347707.2:c.177C>T
CHRNA2 transcript variant 5	NM_001347707.1:c.177=	NM_001347707.1:c.177C>T
CHRNA2 transcript variant 6	NM_001347708.2:c.177=	NM_001347708.2:c.177C>T
CHRNA2 transcript variant 6	NM_001347708.1:c.177=	NM_001347708.1:c.177C>T
CHRNA2 transcript variant X2	XM_047421312.1:c.771=	XM_047421312.1:c.771C>T
CHRNA2 transcript variant X1	XM_047421311.1:c.771=	XM_047421311.1:c.771C>T
CHRNA2 transcript variant X3	XM_047421313.1:c.771=	XM_047421313.1:c.771C>T
neuronal acetylcholine receptor subunit alpha-2 isoform 1 precursor	NP_000733.2:p.Tyr257=	NP_000733.2:p.Tyr257=
neuronal acetylcholine receptor subunit alpha-2 isoform 3	NP_001334635.1:p.Tyr98=	NP_001334635.1:p.Tyr98=
neuronal acetylcholine receptor subunit alpha-2 isoform 2 precursor	NP_001269384.1:p.Tyr242=	NP_001269384.1:p.Tyr242=
neuronal acetylcholine receptor subunit alpha-2 isoform 3	NP_001334634.1:p.Tyr98=	NP_001334634.1:p.Tyr98=
neuronal acetylcholine receptor subunit alpha-2 isoform 4	NP_001334636.1:p.Tyr59=	NP_001334636.1:p.Tyr59=
neuronal acetylcholine receptor subunit alpha-2 isoform 4	NP_001334637.1:p.Tyr59=	NP_001334637.1:p.Tyr59=
neuronal acetylcholine receptor subunit alpha-2 isoform X1	XP_047277268.1:p.Tyr257=	XP_047277268.1:p.Tyr257=
neuronal acetylcholine receptor subunit alpha-2 isoform X1	XP_047277267.1:p.Tyr257=	XP_047277267.1:p.Tyr257=
neuronal acetylcholine receptor subunit alpha-2 isoform X1	XP_047277269.1:p.Tyr257=	XP_047277269.1:p.Tyr257=

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#.

62 SubSNP, 18 Frequency, 5 ClinVar submissions

No	Submitter	Submission ID	Date (Build)
1	UUGC	ss76901686	Dec 07, 2007 (129)
2	PERLEGEN	ss161151683	Dec 01, 2009 (131)
3	1000GENOMES	ss210708330	Jul 14, 2010 (132)
4	1000GENOMES	ss334772661	May 09, 2011 (134)
5	NHLBI-ESP	ss342255734	May 09, 2011 (134)
6	1000GENOMES	ss490962667	May 04, 2012 (137)
7	EXOME_CHIP	ss491411863	May 04, 2012 (137)
8	CLINSEQ_SNP	ss491923165	May 04, 2012 (137)
9	ILLUMINA	ss783476861	Sep 08, 2015 (146)
10	EVA-GONL	ss985336399	Aug 21, 2014 (142)
11	1000GENOMES	ss1329152888	Aug 21, 2014 (142)
12	DDI	ss1431461521	Apr 01, 2015 (144)
13	CLINVAR	ss1457613778	Nov 23, 2014 (142)
14	EVA_FINRISK	ss1584057810	Apr 01, 2015 (144)
15	EVA_DECODE	ss1594929044	Apr 01, 2015 (144)
16	EVA_UK10K_ALSPAC	ss1620263928	Apr 01, 2015 (144)
17	EVA_UK10K_TWINSUK	ss1663257961	Apr 01, 2015 (144)
18	EVA_EXAC	ss1689143428	Apr 01, 2015 (144)
19	EVA_MGP	ss1711197085	Apr 01, 2015 (144)
20	ILLUMINA	ss1752727077	Sep 08, 2015 (146)
21	ILLUMINA	ss1917827147	Feb 12, 2016 (147)
22	WEILL_CORNELL_DGM	ss1928625185	Feb 12, 2016 (147)
23	ILLUMINA	ss1946233313	Feb 12, 2016 (147)
24	ILLUMINA	ss1959099756	Feb 12, 2016 (147)
25	ILLUMINA	ss2094987047	Dec 20, 2016 (150)
26	USC_VALOUEV	ss2153236950	Dec 20, 2016 (150)
27	HUMAN_LONGEVITY	ss2301783588	Dec 20, 2016 (150)
28	GNOMAD	ss2737071313	Nov 08, 2017 (151)
29	GNOMAD	ss2748023062	Nov 08, 2017 (151)
30	GNOMAD	ss2864754037	Nov 08, 2017 (151)
31	AFFY	ss2985435065	Nov 08, 2017 (151)
32	AFFY	ss2986079021	Nov 08, 2017 (151)
33	SWEGEN	ss3002899140	Nov 08, 2017 (151)
34	ILLUMINA	ss3022832459	Nov 08, 2017 (151)
35	CSHL	ss3348109199	Nov 08, 2017 (151)
36	ILLUMINA	ss3635165532	Oct 12, 2018 (152)
37	ILLUMINA	ss3640872822	Oct 12, 2018 (152)
38	ILLUMINA	ss3653373732	Oct 12, 2018 (152)
39	ILLUMINA	ss3654197024	Oct 12, 2018 (152)
40	EGCUT_WGS	ss3670583357	Jul 13, 2019 (153)
41	EVA_DECODE	ss3721677202	Jul 13, 2019 (153)
42	ACPOP	ss3735520102	Jul 13, 2019 (153)
43	ILLUMINA	ss3744578640	Jul 13, 2019 (153)
44	ILLUMINA	ss3745465333	Jul 13, 2019 (153)
45	EVA	ss3767793414	Jul 13, 2019 (153)
46	ILLUMINA	ss3772957866	Jul 13, 2019 (153)
47	EVA	ss3824358558	Apr 26, 2020 (154)
48	EVA	ss3825738743	Apr 26, 2020 (154)
49	SGDP_PRJ	ss3869562656	Apr 26, 2020 (154)
50	FSA-LAB	ss3984396112	Apr 26, 2021 (155)
51	EVA	ss3986418607	Apr 26, 2021 (155)
52	TOPMED	ss4780089182	Apr 26, 2021 (155)
53	EVA	ss5237651167	Oct 16, 2022 (156)
54	1000G_HIGH_COVERAGE	ss5276537773	Oct 16, 2022 (156)
55	EVA	ss5380026129	Oct 16, 2022 (156)
56	1000G_HIGH_COVERAGE	ss5566563849	Oct 16, 2022 (156)
57	SANFORD_IMAGENETICS	ss5645042793	Oct 16, 2022 (156)
58	EVA	ss5830305965	Oct 16, 2022 (156)
59	EVA	ss5848704091	Oct 16, 2022 (156)
60	EVA	ss5888263966	Oct 16, 2022 (156)
61	EVA	ss5974229663	Oct 16, 2022 (156)
62	EVA	ss5980496584	Oct 16, 2022 (156)
63	1000Genomes	NC_000008.10 - 27321189	Oct 12, 2018 (152)
64	1000Genomes_30x	NC_000008.11 - 27463672	Oct 16, 2022 (156)
65	The Avon Longitudinal Study of Parents and Children	NC_000008.10 - 27321189	Oct 12, 2018 (152)
66	Genetic variation in the Estonian population	NC_000008.10 - 27321189	Oct 12, 2018 (152)
67	ExAC	NC_000008.10 - 27321189	Oct 12, 2018 (152)
68	FINRISK	NC_000008.10 - 27321189	Apr 26, 2020 (154)
69	gnomAD - Genomes	NC_000008.11 - 27463672	Apr 26, 2021 (155)
70	gnomAD - Exomes	NC_000008.10 - 27321189	Jul 13, 2019 (153)
71	GO Exome Sequencing Project	NC_000008.10 - 27321189	Oct 12, 2018 (152)
72	Genome of the Netherlands Release 5	NC_000008.10 - 27321189	Apr 26, 2020 (154)
73	Medical Genome Project healthy controls from Spanish population	NC_000008.10 - 27321189	Apr 26, 2020 (154)
74	Northern Sweden	NC_000008.10 - 27321189	Jul 13, 2019 (153)
75	Qatari	NC_000008.10 - 27321189	Apr 26, 2020 (154)
76	SGDP_PRJ	NC_000008.10 - 27321189	Apr 26, 2020 (154)
77	Siberian	NC_000008.10 - 27321189	Apr 26, 2020 (154)
78	TopMed	NC_000008.11 - 27463672	Apr 26, 2021 (155)
79	UK 10K study - Twins	NC_000008.10 - 27321189	Oct 12, 2018 (152)
80	ALFA	NC_000008.11 - 27463672	Apr 26, 2021 (155)
81	ClinVar	RCV000116714.6	Oct 16, 2022 (156)
82	ClinVar	RCV000369041.4	Oct 16, 2022 (156)
83	ClinVar	RCV000460445.7	Oct 16, 2022 (156)
84	ClinVar	RCV000716400.2	Oct 16, 2022 (156)
85	ClinVar	RCV001668226.3	Oct 16, 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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss210708330, ss491923165, ss1594929044, ss2094987047	NC_000008.9:27377105:G:A	NC_000008.11:27463671:G:A	(self)
41255182, 22938968, 16321605, 9239251, 54271, 6241272, 816404, 10249077, 312845, 8804967, 10667115, 21579636, 5753304, 22938968, ss334772661, ss342255734, ss490962667, ss491411863, ss783476861, ss985336399, ss1329152888, ss1431461521, ss1584057810, ss1620263928, ss1663257961, ss1689143428, ss1711197085, ss1752727077, ss1917827147, ss1928625185, ss1946233313, ss1959099756, ss2153236950, ss2737071313, ss2748023062, ss2864754037, ss2985435065, ss2986079021, ss3002899140, ss3022832459, ss3348109199, ss3635165532, ss3640872822, ss3653373732, ss3654197024, ss3670583357, ss3735520102, ss3744578640, ss3745465333, ss3767793414, ss3772957866, ss3824358558, ss3825738743, ss3869562656, ss3984396112, ss3986418607, ss5380026129, ss5645042793, ss5830305965, ss5848704091, ss5974229663, ss5980496584	NC_000008.10:27321188:G:A	NC_000008.11:27463671:G:A	(self)
RCV000116714.6, RCV000369041.4, RCV000460445.7, RCV000716400.2, RCV001668226.3, 54089784, 290884983, 617466742, 10463216628, ss1457613778, ss2301783588, ss3721677202, ss4780089182, ss5237651167, ss5276537773, ss5566563849, ss5888263966	NC_000008.11:27463671:G:A	NC_000008.11:27463671:G:A	(self)
ss76901686, ss161151683	NT_167187.1:15179334:G:A	NC_000008.11:27463671:G:A	(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 rs56229264

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

rs56229264