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rs199473603

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473603(C;T)
Make rs199473603(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38562467
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473603
ebirs199473603
HLIrs199473603
Exacrs199473603
Varsomers199473603
Maprs199473603
PheGenIrs199473603
hapmaprs199473603
1000 genomesrs199473603
hgdprs199473603
ensemblrs199473603
gopubmedrs199473603
geneviewrs199473603
scholarrs199473603
googlers199473603
pharmgkbrs199473603
gwascentralrs199473603
openSNPrs199473603
23andMers199473603
23andMe allrs199473603
SNP Nexus

SNPshotrs199473603
SNPdbers199473603
MSV3drs199473603
GWAS Ctlgrs199473603
Max Magnitude0
ClinVar
Risk rs199473603(T;T)
Alt rs199473603(T;T)
Reference rs199473603(C;C)
Significance Pathogenic
Disease Congenital long QT syndrome Long QT syndrome not provided
Variation info
Gene SCN5A
CLNDBN Congenital long QT syndrome Long QT syndrome not provided
Reversed 1
HGVS NC_000003.11:g.38603958G>A
CLNSRC ClinVar University of Washington
CLNACC RCV000058613.2, RCV000148846.1, RCV000183049.2,