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rs587777559

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(T;T) 0 common in clinvar
Make rs587777559(A;C)
Make rs587777559(C;C)
ReferenceGRCh38 38.1/142
Chromosome11
Position118141315
GeneSCN4B
is asnp
is mentioned by
dbSNPrs587777559
ebirs587777559
HLIrs587777559
Exacrs587777559
Varsomers587777559
Maprs587777559
PheGenIrs587777559
hapmaprs587777559
1000 genomesrs587777559
hgdprs587777559
ensemblrs587777559
gopubmedrs587777559
geneviewrs587777559
scholarrs587777559
googlers587777559
pharmgkbrs587777559
gwascentralrs587777559
openSNPrs587777559
23andMers587777559
23andMe allrs587777559
SNP Nexus

SNPshotrs587777559
SNPdbers587777559
MSV3drs587777559
GWAS Ctlgrs587777559
Max Magnitude0
ClinVar
Risk rs587777559(A,C;A,C)
Alt rs587777559(A,C;A,C)
Reference rs587777559(T;T)
Significance Pathogenic
Disease Atrial fibrillation
Variation info
Gene SCN4B
CLNDBN Atrial fibrillation, familial, 17
Reversed 1
HGVS NC_000011.9:g.118012030A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000128816.2,