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rs587777558

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587777558(C;T)
Make rs587777558(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position123653785
GeneSCN3B
is asnp
is mentioned by
dbSNPrs587777558
ebirs587777558
HLIrs587777558
Exacrs587777558
Varsomers587777558
Maprs587777558
PheGenIrs587777558
hapmaprs587777558
1000 genomesrs587777558
hgdprs587777558
ensemblrs587777558
gopubmedrs587777558
geneviewrs587777558
scholarrs587777558
googlers587777558
pharmgkbrs587777558
gwascentralrs587777558
openSNPrs587777558
23andMers587777558
23andMe allrs587777558
SNP Nexus

SNPshotrs587777558
SNPdbers587777558
MSV3drs587777558
GWAS Ctlgrs587777558
Max Magnitude0
ClinVar
Risk rs587777558(C,T;C,T)
Alt rs587777558(C,T;C,T)
Reference rs587777558(G;G)
Significance Pathogenic
Disease Atrial fibrillation
Variation info
Gene SCN3B
CLNDBN Atrial fibrillation, familial, 16
Reversed 1
HGVS NC_000011.9:g.123524493C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000128815.3,