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rs199473141

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473141(C;C)
Make rs199473141(C;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38598923
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473141
ebirs199473141
HLIrs199473141
Exacrs199473141
Varsomers199473141
Maprs199473141
PheGenIrs199473141
hapmaprs199473141
1000 genomesrs199473141
hgdprs199473141
ensemblrs199473141
gopubmedrs199473141
geneviewrs199473141
scholarrs199473141
googlers199473141
pharmgkbrs199473141
gwascentralrs199473141
openSNPrs199473141
23andMers199473141
23andMe allrs199473141
SNP Nexus

SNPshotrs199473141
SNPdbers199473141
MSV3drs199473141
GWAS Ctlgrs199473141
Max Magnitude0
ClinVar
Risk rs199473141(C;C)
Alt rs199473141(C;C)
Reference rs199473141(T;T)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene SCN5A
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000003.11:g.38640414A>G
CLNSRC ClinVar
CLNACC RCV000058472.2,