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rs587777560

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(T;T) 0 common in clinvar
Make rs587777560(G;G)
Make rs587777560(G;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position118141304
GeneSCN4B
is asnp
is mentioned by
dbSNPrs587777560
ebirs587777560
HLIrs587777560
Exacrs587777560
Varsomers587777560
Maprs587777560
PheGenIrs587777560
hapmaprs587777560
1000 genomesrs587777560
hgdprs587777560
ensemblrs587777560
gopubmedrs587777560
geneviewrs587777560
scholarrs587777560
googlers587777560
pharmgkbrs587777560
gwascentralrs587777560
openSNPrs587777560
23andMers587777560
23andMe allrs587777560
SNP Nexus

SNPshotrs587777560
SNPdbers587777560
MSV3drs587777560
GWAS Ctlgrs587777560
Max Magnitude0
ClinVar
Risk rs587777560(G,T;G,T)
Alt rs587777560(G,T;G,T)
Reference rs587777560(A;A)
Significance Pathogenic
Disease Atrial fibrillation
Variation info
Gene SCN4B
CLNDBN Atrial fibrillation, familial, 17
Reversed 1
HGVS NC_000011.9:g.118012019T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000128817.2,