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rs587777336

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587777336(A;G)
Make rs587777336(G;G)
ReferenceGRCh38 38.1/142
Chromosome12
Position5044290
GeneKCNA5
is asnp
is mentioned by
dbSNPrs587777336
ebirs587777336
HLIrs587777336
Exacrs587777336
Varsomers587777336
Maprs587777336
PheGenIrs587777336
hapmaprs587777336
1000 genomesrs587777336
hgdprs587777336
ensemblrs587777336
gopubmedrs587777336
geneviewrs587777336
scholarrs587777336
googlers587777336
pharmgkbrs587777336
gwascentralrs587777336
openSNPrs587777336
23andMers587777336
23andMe allrs587777336
SNP Nexus

SNPshotrs587777336
SNPdbers587777336
MSV3drs587777336
GWAS Ctlgrs587777336
Max Magnitude0
ClinVar
Risk rs587777336(G;G)
Alt rs587777336(G;G)
Reference rs587777336(A;A)
Significance Pathogenic
Disease Atrial fibrillation
Variation info
Gene KCNA5
CLNDBN Atrial fibrillation, familial, 7
Reversed 0
HGVS NC_000012.11:g.5153456A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000114991.3,