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rs387906614

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906614(A;A)
Make rs387906614(A;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position147758578
GeneGJA5
is asnp
is mentioned by
dbSNPrs387906614
ebirs387906614
HLIrs387906614
Exacrs387906614
Varsomers387906614
Maprs387906614
PheGenIrs387906614
hapmaprs387906614
1000 genomesrs387906614
hgdprs387906614
ensemblrs387906614
gopubmedrs387906614
geneviewrs387906614
scholarrs387906614
googlers387906614
pharmgkbrs387906614
gwascentralrs387906614
openSNPrs387906614
23andMers387906614
23andMe allrs387906614
SNP Nexus

SNPshotrs387906614
SNPdbers387906614
MSV3drs387906614
GWAS Ctlgrs387906614
Max Magnitude0
ClinVar
Risk rs387906614(A;A)
Alt rs387906614(A;A)
Reference rs387906614(C;C)
Significance Pathogenic
Disease Atrial fibrillation
Variation info
Gene GJA5
CLNDBN Atrial fibrillation, familial, 11
Reversed 1
HGVS NC_000001.10:g.147230686G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000022514.27,