Name: rs74772771
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.

rs74772771

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr8:27469915 (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 / G>C
Variation Type: SNV Single Nucleotide Variation
Frequency: A=0.000329 (87/264690, TOPMED)
A=0.000595 (118/198440, ALFA)
A=0.000364 (51/140284, GnomAD) (+ 8 more)
A=0.00014 (11/78698, PAGE_STUDY)
A=0.00023 (3/13006, GO-ESP)
A=0.0005 (3/6404, 1000G_30x)
A=0.0004 (2/5008, 1000G)
A=0.0008 (3/3854, ALSPAC)
A=0.0005 (2/3708, TWINSUK)
A=0.001 (1/998, GoNL)
A=0.002 (1/534, MGP)

Clinical Significance: Reported in ClinVar
Gene : Consequence: CHRNA2 : Missense 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	214850	G=0.999418	A=0.000582
European	Sub	179862	G=0.999344	A=0.000656
African	Sub	9358	G=1.0000	A=0.0000
African Others	Sub	360	G=1.000	A=0.000
African American	Sub	8998	G=1.0000	A=0.0000
Asian	Sub	6312	G=1.0000	A=0.0000
East Asian	Sub	4466	G=1.0000	A=0.0000
Other Asian	Sub	1846	G=1.0000	A=0.0000
Latin American 1	Sub	790	G=1.000	A=0.000
Latin American 2	Sub	966	G=1.000	A=0.000
South Asian	Sub	274	G=1.000	A=0.000
Other	Sub	17288	G=0.99960	A=0.00040

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=0.999671	A=0.000329
Allele Frequency Aggregator	Total	Global	198440	G=0.999405	A=0.000595
Allele Frequency Aggregator	European	Sub	169724	G=0.999346	A=0.000654
Allele Frequency Aggregator	Other	Sub	15854	G=0.99956	A=0.00044
Allele Frequency Aggregator	Asian	Sub	6312	G=1.0000	A=0.0000
Allele Frequency Aggregator	African	Sub	4520	G=1.0000	A=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	966	G=1.000	A=0.000
Allele Frequency Aggregator	Latin American 1	Sub	790	G=1.000	A=0.000
Allele Frequency Aggregator	South Asian	Sub	274	G=1.000	A=0.000
gnomAD - Genomes	Global	Study-wide	140284	G=0.999636	A=0.000364
gnomAD - Genomes	European	Sub	75956	G=0.99943	A=0.00057
gnomAD - Genomes	African	Sub	42056	G=0.99988	A=0.00012
gnomAD - Genomes	American	Sub	13662	G=0.99985	A=0.00015
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	G=1.0000	A=0.0000
gnomAD - Genomes	East Asian	Sub	3132	G=1.0000	A=0.0000
gnomAD - Genomes	Other	Sub	2154	G=0.9995	A=0.0005
The PAGE Study	Global	Study-wide	78698	G=0.99986	A=0.00014
The PAGE Study	AfricanAmerican	Sub	32514	G=0.99985	A=0.00015
The PAGE Study	Mexican	Sub	10810	G=0.99991	A=0.00009
The PAGE Study	Asian	Sub	8316	G=0.9999	A=0.0001
The PAGE Study	PuertoRican	Sub	7918	G=0.9999	A=0.0001
The PAGE Study	NativeHawaiian	Sub	4534	G=0.9996	A=0.0004
The PAGE Study	Cuban	Sub	4230	G=1.0000	A=0.0000
The PAGE Study	Dominican	Sub	3828	G=1.0000	A=0.0000
The PAGE Study	CentralAmerican	Sub	2450	G=1.0000	A=0.0000
The PAGE Study	SouthAmerican	Sub	1982	G=0.9995	A=0.0005
The PAGE Study	NativeAmerican	Sub	1260	G=1.0000	A=0.0000
The PAGE Study	SouthAsian	Sub	856	G=1.000	A=0.000
GO Exome Sequencing Project	Global	Study-wide	13006	G=0.99977	A=0.00023
GO Exome Sequencing Project	European American	Sub	8600	G=0.9997	A=0.0003
GO Exome Sequencing Project	African American	Sub	4406	G=1.0000	A=0.0000
1000Genomes_30x	Global	Study-wide	6404	G=0.9995	A=0.0005
1000Genomes_30x	African	Sub	1786	G=1.0000	A=0.0000
1000Genomes_30x	Europe	Sub	1266	G=0.9984	A=0.0016
1000Genomes_30x	South Asian	Sub	1202	G=1.0000	A=0.0000
1000Genomes_30x	East Asian	Sub	1170	G=1.0000	A=0.0000
1000Genomes_30x	American	Sub	980	G=0.999	A=0.001
1000Genomes	Global	Study-wide	5008	G=0.9996	A=0.0004
1000Genomes	African	Sub	1322	G=1.0000	A=0.0000
1000Genomes	East Asian	Sub	1008	G=1.0000	A=0.0000
1000Genomes	Europe	Sub	1006	G=0.9990	A=0.0010
1000Genomes	South Asian	Sub	978	G=1.000	A=0.000
1000Genomes	American	Sub	694	G=0.999	A=0.001
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	G=0.9992	A=0.0008
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	G=0.9995	A=0.0005
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	G=0.999	A=0.001
Medical Genome Project healthy controls from Spanish population	Spanish controls	Study-wide	534	G=0.998	A=0.002

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.27469915G>A
GRCh38.p14 chr 8	NC_000008.11:g.27469915G>C
GRCh37.p13 chr 8	NC_000008.10:g.27327432G>A
GRCh37.p13 chr 8	NC_000008.10:g.27327432G>C
CHRNA2 RefSeqGene	NG_015827.1:g.14382C>T
CHRNA2 RefSeqGene	NG_015827.1:g.14382C>G

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

Molecule type	Change	Amino acid[Codon]	SO Term
CHRNA2 transcript variant 3	NM_001347705.2:c.-288=	N/A	5 Prime UTR Variant
CHRNA2 transcript variant 6	NM_001347708.2:c.-322=	N/A	5 Prime UTR Variant
CHRNA2 transcript variant 5	NM_001347707.2:c.-274=	N/A	5 Prime UTR Variant
CHRNA2 transcript variant 4	NM_001347706.2:c.-333=	N/A	5 Prime UTR Variant
CHRNA2 transcript variant 1	NM_000742.4:c.140C>T	T [ACG] > M [ATG]	Coding Sequence Variant
neuronal acetylcholine receptor subunit alpha-2 isoform 1 precursor	NP_000733.2:p.Thr47Met	T (Thr) > M (Met)	Missense Variant
CHRNA2 transcript variant 1	NM_000742.4:c.140C>G	T [ACG] > R [AGG]	Coding Sequence Variant
neuronal acetylcholine receptor subunit alpha-2 isoform 1 precursor	NP_000733.2:p.Thr47Arg	T (Thr) > R (Arg)	Missense Variant
CHRNA2 transcript variant 2	NM_001282455.2:c.140C>T	T [ACG] > M [ATG]	Coding Sequence Variant
neuronal acetylcholine receptor subunit alpha-2 isoform 2 precursor	NP_001269384.1:p.Thr47Met	T (Thr) > M (Met)	Missense Variant
CHRNA2 transcript variant 2	NM_001282455.2:c.140C>G	T [ACG] > R [AGG]	Coding Sequence Variant
neuronal acetylcholine receptor subunit alpha-2 isoform 2 precursor	NP_001269384.1:p.Thr47Arg	T (Thr) > R (Arg)	Missense Variant
CHRNA2 transcript variant X1	XM_047421311.1:c.140C>T	T [ACG] > M [ATG]	Coding Sequence Variant
neuronal acetylcholine receptor subunit alpha-2 isoform X1	XP_047277267.1:p.Thr47Met	T (Thr) > M (Met)	Missense Variant
CHRNA2 transcript variant X1	XM_047421311.1:c.140C>G	T [ACG] > R [AGG]	Coding Sequence Variant
neuronal acetylcholine receptor subunit alpha-2 isoform X1	XP_047277267.1:p.Thr47Arg	T (Thr) > R (Arg)	Missense Variant
CHRNA2 transcript variant X2	XM_047421312.1:c.140C>T	T [ACG] > M [ATG]	Coding Sequence Variant
neuronal acetylcholine receptor subunit alpha-2 isoform X1	XP_047277268.1:p.Thr47Met	T (Thr) > M (Met)	Missense Variant
CHRNA2 transcript variant X2	XM_047421312.1:c.140C>G	T [ACG] > R [AGG]	Coding Sequence Variant
neuronal acetylcholine receptor subunit alpha-2 isoform X1	XP_047277268.1:p.Thr47Arg	T (Thr) > R (Arg)	Missense Variant
CHRNA2 transcript variant X3	XM_047421313.1:c.140C>T	T [ACG] > M [ATG]	Coding Sequence Variant
neuronal acetylcholine receptor subunit alpha-2 isoform X1	XP_047277269.1:p.Thr47Met	T (Thr) > M (Met)	Missense Variant
CHRNA2 transcript variant X3	XM_047421313.1:c.140C>G	T [ACG] > R [AGG]	Coding Sequence Variant
neuronal acetylcholine receptor subunit alpha-2 isoform X1	XP_047277269.1:p.Thr47Arg	T (Thr) > R (Arg)	Missense 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: 202268 )

ClinVar Accession	Disease Names	Clinical Significance
RCV000615228.6	Autosomal dominant nocturnal frontal lobe epilepsy 4	Conflicting-Interpretations-Of-Pathogenicity
RCV000727343.16	not provided	Conflicting-Interpretations-Of-Pathogenicity
RCV001079768.4	Autosomal dominant nocturnal frontal lobe epilepsy	Likely-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	C
GRCh38.p14 chr 8	NC_000008.11:g.27469915=	NC_000008.11:g.27469915G>A	NC_000008.11:g.27469915G>C
GRCh37.p13 chr 8	NC_000008.10:g.27327432=	NC_000008.10:g.27327432G>A	NC_000008.10:g.27327432G>C
CHRNA2 RefSeqGene	NG_015827.1:g.14382=	NG_015827.1:g.14382C>T	NG_015827.1:g.14382C>G
CHRNA2 transcript variant 1	NM_000742.4:c.140=	NM_000742.4:c.140C>T	NM_000742.4:c.140C>G
CHRNA2 transcript variant 1	NM_000742.3:c.140=	NM_000742.3:c.140C>T	NM_000742.3:c.140C>G
CHRNA2 transcript variant 4	NM_001347706.2:c.-333=	NM_001347706.2:c.-333C>T	NM_001347706.2:c.-333C>G
CHRNA2 transcript variant 4	NM_001347706.1:c.-333=	NM_001347706.1:c.-333C>T	NM_001347706.1:c.-333C>G
CHRNA2 transcript variant 2	NM_001282455.2:c.140=	NM_001282455.2:c.140C>T	NM_001282455.2:c.140C>G
CHRNA2 transcript variant 2	NM_001282455.1:c.140=	NM_001282455.1:c.140C>T	NM_001282455.1:c.140C>G
CHRNA2 transcript variant 3	NM_001347705.2:c.-288=	NM_001347705.2:c.-288C>T	NM_001347705.2:c.-288C>G
CHRNA2 transcript variant 3	NM_001347705.1:c.-288=	NM_001347705.1:c.-288C>T	NM_001347705.1:c.-288C>G
CHRNA2 transcript variant 5	NM_001347707.2:c.-274=	NM_001347707.2:c.-274C>T	NM_001347707.2:c.-274C>G
CHRNA2 transcript variant 5	NM_001347707.1:c.-274=	NM_001347707.1:c.-274C>T	NM_001347707.1:c.-274C>G
CHRNA2 transcript variant 6	NM_001347708.2:c.-322=	NM_001347708.2:c.-322C>T	NM_001347708.2:c.-322C>G
CHRNA2 transcript variant 6	NM_001347708.1:c.-322=	NM_001347708.1:c.-322C>T	NM_001347708.1:c.-322C>G
CHRNA2 transcript variant X2	XM_047421312.1:c.140=	XM_047421312.1:c.140C>T	XM_047421312.1:c.140C>G
CHRNA2 transcript variant X1	XM_047421311.1:c.140=	XM_047421311.1:c.140C>T	XM_047421311.1:c.140C>G
CHRNA2 transcript variant X3	XM_047421313.1:c.140=	XM_047421313.1:c.140C>T	XM_047421313.1:c.140C>G
neuronal acetylcholine receptor subunit alpha-2 isoform 1 precursor	NP_000733.2:p.Thr47=	NP_000733.2:p.Thr47Met	NP_000733.2:p.Thr47Arg
neuronal acetylcholine receptor subunit alpha-2 isoform 2 precursor	NP_001269384.1:p.Thr47=	NP_001269384.1:p.Thr47Met	NP_001269384.1:p.Thr47Arg
neuronal acetylcholine receptor subunit alpha-2 isoform X1	XP_047277268.1:p.Thr47=	XP_047277268.1:p.Thr47Met	XP_047277268.1:p.Thr47Arg
neuronal acetylcholine receptor subunit alpha-2 isoform X1	XP_047277267.1:p.Thr47=	XP_047277267.1:p.Thr47Met	XP_047277267.1:p.Thr47Arg
neuronal acetylcholine receptor subunit alpha-2 isoform X1	XP_047277269.1:p.Thr47=	XP_047277269.1:p.Thr47Met	XP_047277269.1:p.Thr47Arg

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#.

45 SubSNP, 15 Frequency, 3 ClinVar submissions

No	Submitter	Submission ID	Date (Build)
1	PERLEGEN	ss161151701	Dec 01, 2009 (131)
2	1000GENOMES	ss488885922	May 04, 2012 (137)
3	EXOME_CHIP	ss491411870	May 04, 2012 (137)
4	CLINSEQ_SNP	ss491923172	May 04, 2012 (137)
5	NHLBI-ESP	ss712834855	Apr 25, 2013 (138)
6	ILLUMINA	ss780868673	Sep 08, 2015 (146)
7	ILLUMINA	ss783553672	Sep 08, 2015 (146)
8	EVA-GONL	ss985336453	Aug 21, 2014 (142)
9	1000GENOMES	ss1329153094	Aug 21, 2014 (142)
10	EVA_DECODE	ss1594929110	Apr 01, 2015 (144)
11	EVA_UK10K_ALSPAC	ss1620264052	Apr 01, 2015 (144)
12	EVA_UK10K_TWINSUK	ss1663258085	Apr 01, 2015 (144)
13	EVA_EXAC	ss1689143630	Apr 01, 2015 (144)
14	EVA_EXAC	ss1689143631	Apr 01, 2015 (144)
15	EVA_MGP	ss1711197094	Apr 01, 2015 (144)
16	ILLUMINA	ss1752727086	Sep 08, 2015 (146)
17	ILLUMINA	ss1917827152	Feb 12, 2016 (147)
18	ILLUMINA	ss1946233320	Feb 12, 2016 (147)
19	ILLUMINA	ss1959099771	Feb 12, 2016 (147)
20	HUMAN_LONGEVITY	ss2301783998	Dec 20, 2016 (150)
21	GNOMAD	ss2737071601	Nov 08, 2017 (151)
22	GNOMAD	ss2748023160	Nov 08, 2017 (151)
23	GNOMAD	ss2864754560	Nov 08, 2017 (151)
24	AFFY	ss2985435074	Nov 08, 2017 (151)
25	AFFY	ss2986079056	Nov 08, 2017 (151)
26	SWEGEN	ss3002899215	Nov 08, 2017 (151)
27	ILLUMINA	ss3630028361	Oct 12, 2018 (152)
28	ILLUMINA	ss3635165541	Oct 12, 2018 (152)
29	ILLUMINA	ss3640872831	Oct 12, 2018 (152)
30	ILLUMINA	ss3644966506	Oct 12, 2018 (152)
31	ILLUMINA	ss3654197033	Oct 12, 2018 (152)
32	EVA_DECODE	ss3721677284	Jul 13, 2019 (153)
33	ILLUMINA	ss3744578645	Jul 13, 2019 (153)
34	ILLUMINA	ss3745465342	Jul 13, 2019 (153)
35	PAGE_CC	ss3771433264	Jul 13, 2019 (153)
36	ILLUMINA	ss3772957875	Jul 13, 2019 (153)
37	EVA	ss3824358601	Apr 26, 2020 (154)
38	TOPMED	ss4780090788	Apr 26, 2021 (155)
39	1000G_HIGH_COVERAGE	ss5276537939	Oct 16, 2022 (156)
40	EVA	ss5380026461	Oct 16, 2022 (156)
41	HUGCELL_USP	ss5473169162	Oct 16, 2022 (156)
42	1000G_HIGH_COVERAGE	ss5566564097	Oct 16, 2022 (156)
43	EVA	ss5848171969	Oct 16, 2022 (156)
44	EVA	ss5888264173	Oct 16, 2022 (156)
45	EVA	ss5974229778	Oct 16, 2022 (156)
46	1000Genomes	NC_000008.10 - 27327432	Oct 12, 2018 (152)
47	1000Genomes_30x	NC_000008.11 - 27469915	Oct 16, 2022 (156)
48	The Avon Longitudinal Study of Parents and Children	NC_000008.10 - 27327432	Oct 12, 2018 (152)
49	ExAC Submission ignored due to conflicting rows: Row 9239463 (NC_000008.10:27327431:G:G 120824/120884, NC_000008.10:27327431:G:A 60/120884) Row 9239464 (NC_000008.10:27327431:G:G 120883/120884, NC_000008.10:27327431:G:C 1/120884)	-	Oct 12, 2018 (152)
50	ExAC Submission ignored due to conflicting rows: Row 9239463 (NC_000008.10:27327431:G:G 120824/120884, NC_000008.10:27327431:G:A 60/120884) Row 9239464 (NC_000008.10:27327431:G:G 120883/120884, NC_000008.10:27327431:G:C 1/120884)	-	Oct 12, 2018 (152)
51	gnomAD - Genomes	NC_000008.11 - 27469915	Apr 26, 2021 (155)
52	gnomAD - Exomes Submission ignored due to conflicting rows: Row 6241568 (NC_000008.10:27327431:G:G 251128/251244, NC_000008.10:27327431:G:A 116/251244) Row 6241569 (NC_000008.10:27327431:G:G 251243/251244, NC_000008.10:27327431:G:C 1/251244)	-	Jul 13, 2019 (153)
53	gnomAD - Exomes Submission ignored due to conflicting rows: Row 6241568 (NC_000008.10:27327431:G:G 251128/251244, NC_000008.10:27327431:G:A 116/251244) Row 6241569 (NC_000008.10:27327431:G:G 251243/251244, NC_000008.10:27327431:G:C 1/251244)	-	Jul 13, 2019 (153)
54	GO Exome Sequencing Project	NC_000008.10 - 27327432	Oct 12, 2018 (152)
55	Genome of the Netherlands Release 5	NC_000008.10 - 27327432	Apr 26, 2020 (154)
56	Medical Genome Project healthy controls from Spanish population	NC_000008.10 - 27327432	Apr 26, 2020 (154)
57	The PAGE Study	NC_000008.11 - 27469915	Jul 13, 2019 (153)
58	TopMed	NC_000008.11 - 27469915	Apr 26, 2021 (155)
59	UK 10K study - Twins	NC_000008.10 - 27327432	Oct 12, 2018 (152)
60	ALFA	NC_000008.11 - 27469915	Apr 26, 2021 (155)
61	ClinVar	RCV000615228.6	Oct 16, 2022 (156)
62	ClinVar	RCV000727343.16	Oct 16, 2022 (156)
63	ClinVar	RCV001079768.4	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
ss491923172, ss1594929110	NC_000008.9:27383348:G:A	NC_000008.11:27469914:G:A	(self)
41255395, 22939096, 816447, 10249131, 312854, 22939096, ss488885922, ss491411870, ss712834855, ss780868673, ss783553672, ss985336453, ss1329153094, ss1620264052, ss1663258085, ss1689143630, ss1711197094, ss1752727086, ss1917827152, ss1946233320, ss1959099771, ss2737071601, ss2748023160, ss2864754560, ss2985435074, ss2986079056, ss3002899215, ss3630028361, ss3635165541, ss3640872831, ss3644966506, ss3654197033, ss3744578645, ss3745465342, ss3772957875, ss3824358601, ss5380026461, ss5848171969, ss5974229778	NC_000008.10:27327431:G:A	NC_000008.11:27469914:G:A	(self)
RCV000615228.6, RCV000727343.16, RCV001079768.4, 54090032, 290886248, 654733, 617468348, 5489511616, ss2301783998, ss3721677284, ss3771433264, ss4780090788, ss5276537939, ss5473169162, ss5566564097, ss5888264173	NC_000008.11:27469914:G:A	NC_000008.11:27469914:G:A	(self)
ss161151701	NT_167187.1:15185577:G:A	NC_000008.11:27469914:G:A	(self)
ss1689143631, ss2737071601	NC_000008.10:27327431:G:C	NC_000008.11:27469914:G: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 rs74772771

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

rs74772771