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rs796052317

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052317(C;C)
Make rs796052317(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63350867
GeneCHRNA4
is asnp
is mentioned by
dbSNPrs796052317
ebirs796052317
HLIrs796052317
Exacrs796052317
Varsomers796052317
Maprs796052317
PheGenIrs796052317
hapmaprs796052317
1000 genomesrs796052317
hgdprs796052317
ensemblrs796052317
gopubmedrs796052317
geneviewrs796052317
scholarrs796052317
googlers796052317
pharmgkbrs796052317
gwascentralrs796052317
openSNPrs796052317
23andMers796052317
23andMe allrs796052317
SNP Nexus

SNPshotrs796052317
SNPdbers796052317
MSV3drs796052317
GWAS Ctlgrs796052317
Max Magnitude0
ClinVar
Risk rs796052317(C;C)
Alt rs796052317(C;C)
Reference rs796052317(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CHRNA4
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.61982219A>G
CLNSRC
CLNACC RCV000186925.1,