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rs387906612

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906612(C;T)
Make rs387906612(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position147759094
GeneGJA5
is asnp
is mentioned by
dbSNPrs387906612
ebirs387906612
HLIrs387906612
Exacrs387906612
Varsomers387906612
Maprs387906612
PheGenIrs387906612
hapmaprs387906612
1000 genomesrs387906612
hgdprs387906612
ensemblrs387906612
gopubmedrs387906612
geneviewrs387906612
scholarrs387906612
googlers387906612
pharmgkbrs387906612
gwascentralrs387906612
openSNPrs387906612
23andMers387906612
23andMe allrs387906612
SNP Nexus

SNPshotrs387906612
SNPdbers387906612
MSV3drs387906612
GWAS Ctlgrs387906612
Max Magnitude0
ClinVar
Risk rs387906612(T;T)
Alt rs387906612(T;T)
Reference rs387906612(C;C)
Significance Pathogenic
Disease Atrial fibrillation
Variation info
Gene GJA5
CLNDBN Atrial fibrillation, familial, 11
Reversed 1
HGVS NC_000001.10:g.147231202G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000022512.29,