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rs387906613

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906613(A;A)
Make rs387906613(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position147758986
GeneGJA5
is asnp
is mentioned by
dbSNPrs387906613
ebirs387906613
HLIrs387906613
Exacrs387906613
Varsomers387906613
Maprs387906613
PheGenIrs387906613
hapmaprs387906613
1000 genomesrs387906613
hgdprs387906613
ensemblrs387906613
gopubmedrs387906613
geneviewrs387906613
scholarrs387906613
googlers387906613
pharmgkbrs387906613
gwascentralrs387906613
openSNPrs387906613
23andMers387906613
23andMe allrs387906613
SNP Nexus

SNPshotrs387906613
SNPdbers387906613
MSV3drs387906613
GWAS Ctlgrs387906613
Max Magnitude0
ClinVar
Risk rs387906613(A,T;A,T)
Alt rs387906613(A,T;A,T)
Reference rs387906613(G;G)
Significance Pathogenic
Disease Atrial fibrillation
Variation info
Gene GJA5
CLNDBN Atrial fibrillation, familial, 11
Reversed 1
HGVS NC_000001.10:g.147231094C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000022513.27,