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rs387906615

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906615(A;A)
Make rs387906615(A;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position147758554
GeneGJA5
is asnp
is mentioned by
dbSNPrs387906615
ebirs387906615
HLIrs387906615
Exacrs387906615
Varsomers387906615
Maprs387906615
PheGenIrs387906615
hapmaprs387906615
1000 genomesrs387906615
hgdprs387906615
ensemblrs387906615
gopubmedrs387906615
geneviewrs387906615
scholarrs387906615
googlers387906615
pharmgkbrs387906615
gwascentralrs387906615
openSNPrs387906615
23andMers387906615
23andMe allrs387906615
SNP Nexus

SNPshotrs387906615
SNPdbers387906615
MSV3drs387906615
GWAS Ctlgrs387906615
Max Magnitude0
ClinVar
Risk rs387906615(A;A)
Alt rs387906615(A;A)
Reference rs387906615(C;C)
Significance Pathogenic
Disease Atrial fibrillation
Variation info
Gene GJA5
CLNDBN Atrial fibrillation, familial, 11
Reversed 1
HGVS NC_000001.10:g.147230662G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000022515.24,