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rs199473579

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473579(A;A)
Make rs199473579(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position38598978
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473579
ebirs199473579
HLIrs199473579
Exacrs199473579
Varsomers199473579
Maprs199473579
PheGenIrs199473579
hapmaprs199473579
1000 genomesrs199473579
hgdprs199473579
ensemblrs199473579
gopubmedrs199473579
geneviewrs199473579
scholarrs199473579
googlers199473579
pharmgkbrs199473579
gwascentralrs199473579
openSNPrs199473579
23andMers199473579
23andMe allrs199473579
SNP Nexus

SNPshotrs199473579
SNPdbers199473579
MSV3drs199473579
GWAS Ctlgrs199473579
Max Magnitude0
ClinVar
Risk rs199473579(A;A)
Alt rs199473579(A;A)
Reference rs199473579(G;G)
Significance Pathogenic
Disease Atrial fibrillation Atrial fibrillation
Variation info
Gene SCN5A
CLNDBN Atrial fibrillation, familial, 10 Atrial fibrillation
Reversed 1
HGVS NC_000003.11:g.38640469C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000022951.2, RCV000058468.2,


[PMID 18378609OA-icon.png] Cardiac sodium channel (SCN5A) variants associated with atrial fibrillation.