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rs2302763

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs2302763(C;C)
Make rs2302763(C;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position7455958
GeneCHRNB1
is asnp
is mentioned by
dbSNPrs2302763
dbSNP (classic)rs2302763
ClinGenrs2302763
ebirs2302763
HLIrs2302763
Exacrs2302763
Gnomadrs2302763
Varsomers2302763
LitVarrs2302763
Maprs2302763
PheGenIrs2302763
Biobankrs2302763
1000 genomesrs2302763
hgdprs2302763
ensemblrs2302763
geneviewrs2302763
scholarrs2302763
googlers2302763
pharmgkbrs2302763
gwascentralrs2302763
openSNPrs2302763
23andMers2302763
SNPshotrs2302763
SNPdbers2302763
MSV3drs2302763
GWAS Ctlgrs2302763
GMAF0.1717
Max Magnitude0
? (C;C) (C;T) (T;T) 28


Variations in this snp have been linked to nicotine dependence [PMID 16874522]


[PMID 19259974OA-icon.png] Multiple distinct risk loci for nicotine dependence identified by dense coverage of the complete family of nicotinic receptor subunit (CHRN) genes.


ClinVar
Risk rs2302763(C;C)
Alt rs2302763(C;C)
Reference Rs2302763(T;T)
Significance Non-pathogenic
Disease not specified
Variation info
Gene CHRNB1
CLNDBN not specified
Reversed 0
HGVS NC_000017.10:g.7359277T>C
CLNSRC
CLNACC RCV000242294.2,