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rs587777556

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777556(A;A)
Make rs587777556(A;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position123642502
GeneSCN3B
is asnp
is mentioned by
dbSNPrs587777556
ebirs587777556
HLIrs587777556
Exacrs587777556
Varsomers587777556
Maprs587777556
PheGenIrs587777556
hapmaprs587777556
1000 genomesrs587777556
hgdprs587777556
ensemblrs587777556
gopubmedrs587777556
geneviewrs587777556
scholarrs587777556
googlers587777556
pharmgkbrs587777556
gwascentralrs587777556
openSNPrs587777556
23andMers587777556
23andMe allrs587777556
SNP Nexus

SNPshotrs587777556
SNPdbers587777556
MSV3drs587777556
GWAS Ctlgrs587777556
Max Magnitude0
ClinVar
Risk rs587777556(A;A)
Alt rs587777556(A;A)
Reference rs587777556(G;G)
Significance Pathogenic
Disease Atrial fibrillation
Variation info
Gene SCN3B
CLNDBN Atrial fibrillation, familial, 16
Reversed 0
HGVS NC_000011.9:g.123513210G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000128813.3,