Have questions? Visit https://www.reddit.com/r/SNPedia

rs587777557

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587777557(A;G)
Make rs587777557(G;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position123638288
GeneSCN3B
is asnp
is mentioned by
dbSNPrs587777557
ebirs587777557
HLIrs587777557
Exacrs587777557
Varsomers587777557
Maprs587777557
PheGenIrs587777557
hapmaprs587777557
1000 genomesrs587777557
hgdprs587777557
ensemblrs587777557
gopubmedrs587777557
geneviewrs587777557
scholarrs587777557
googlers587777557
pharmgkbrs587777557
gwascentralrs587777557
openSNPrs587777557
23andMers587777557
23andMe allrs587777557
SNP Nexus

SNPshotrs587777557
SNPdbers587777557
MSV3drs587777557
GWAS Ctlgrs587777557
Max Magnitude0
ClinVar
Risk rs587777557(G;G)
Alt rs587777557(G;G)
Reference rs587777557(A;A)
Significance Pathogenic
Disease Atrial fibrillation
Variation info
Gene SCN3B
CLNDBN Atrial fibrillation, familial, 16
Reversed 0
HGVS NC_000011.9:g.123508996A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000128814.3,