Have questions? Visit https://www.reddit.com/r/SNPedia

rs199473581

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473581(G;T)
Make rs199473581(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38597865
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473581
ebirs199473581
HLIrs199473581
Exacrs199473581
Varsomers199473581
Maprs199473581
PheGenIrs199473581
hapmaprs199473581
1000 genomesrs199473581
hgdprs199473581
ensemblrs199473581
gopubmedrs199473581
geneviewrs199473581
scholarrs199473581
googlers199473581
pharmgkbrs199473581
gwascentralrs199473581
openSNPrs199473581
23andMers199473581
23andMe allrs199473581
SNP Nexus

SNPshotrs199473581
SNPdbers199473581
MSV3drs199473581
GWAS Ctlgrs199473581
Max Magnitude0
ClinVar
Risk rs199473581(T;T)
Alt rs199473581(T;T)
Reference rs199473581(G;G)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene SCN5A
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000003.11:g.38639356C>A
CLNSRC ClinVar
CLNACC RCV000058483.2,