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rs587777304

From SNPedia

Orientationplus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
(T;T) 0 common in clinvar
Make rs587777304(A;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position147759016
GeneGJA5, LOC102723321
is asnp
is mentioned by
dbSNPrs587777304
dbSNP (old)rs587777304
ClinGenrs587777304
ebirs587777304
HLIrs587777304
Exacrs587777304
Varsomers587777304
Maprs587777304
PheGenIrs587777304
Biobankrs587777304
1000 genomesrs587777304
hgdprs587777304
ensemblrs587777304
gopubmedrs587777304
geneviewrs587777304
scholarrs587777304
googlers587777304
pharmgkbrs587777304
gwascentralrs587777304
openSNPrs587777304
23andMers587777304
23andMe allrs587777304
SNP Nexus

SNPshotrs587777304
SNPdbers587777304
MSV3drs587777304
GWAS Ctlgrs587777304
Max Magnitude0
ClinVar
Risk Rs587777304(T;T)
Alt Rs587777304(T;T)
Reference Rs587777304(A;A)
Significance Pathogenic
Disease Atrial fibrillation
Variation info
Gene GJA5
CLNDBN Atrial fibrillation, familial, 11
Reversed 1
HGVS NC_000001.10:g.147231124T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000114757.2,