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rs199473197

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473197(C;T)
Make rs199473197(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38576780
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473197
ebirs199473197
HLIrs199473197
Exacrs199473197
Varsomers199473197
Maprs199473197
PheGenIrs199473197
hapmaprs199473197
1000 genomesrs199473197
hgdprs199473197
ensemblrs199473197
gopubmedrs199473197
geneviewrs199473197
scholarrs199473197
googlers199473197
pharmgkbrs199473197
gwascentralrs199473197
openSNPrs199473197
23andMers199473197
23andMe allrs199473197
SNP Nexus

SNPshotrs199473197
SNPdbers199473197
MSV3drs199473197
GWAS Ctlgrs199473197
Max Magnitude0
ClinVar
Risk rs199473197(T;T)
Alt rs199473197(T;T)
Reference rs199473197(C;C)
Significance Pathogenic
Disease Atrial fibrillation not provided
Variation info
Gene SCN5A
CLNDBN Atrial fibrillation not provided
Reversed 1
HGVS NC_000003.11:g.38618271G>A
CLNSRC ClinVar
CLNACC RCV000058569.2, RCV000183033.1,