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

rs199473126

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473126(G;T)
Make rs199473126(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38603890
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473126
ebirs199473126
HLIrs199473126
Exacrs199473126
Varsomers199473126
Maprs199473126
PheGenIrs199473126
hapmaprs199473126
1000 genomesrs199473126
hgdprs199473126
ensemblrs199473126
gopubmedrs199473126
geneviewrs199473126
scholarrs199473126
googlers199473126
pharmgkbrs199473126
gwascentralrs199473126
openSNPrs199473126
23andMers199473126
23andMe allrs199473126
SNP Nexus

SNPshotrs199473126
SNPdbers199473126
MSV3drs199473126
GWAS Ctlgrs199473126
Max Magnitude0
ClinVar
Risk rs199473126(T;T)
Alt rs199473126(T;T)
Reference rs199473126(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.38645381C>A
CLNSRC ClinVar
CLNACC RCV000058445.2,