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

rs199473591

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473591(G;T)
Make rs199473591(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38581217
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473591
ebirs199473591
HLIrs199473591
Exacrs199473591
Varsomers199473591
Maprs199473591
PheGenIrs199473591
hapmaprs199473591
1000 genomesrs199473591
hgdprs199473591
ensemblrs199473591
gopubmedrs199473591
geneviewrs199473591
scholarrs199473591
googlers199473591
pharmgkbrs199473591
gwascentralrs199473591
openSNPrs199473591
23andMers199473591
23andMe allrs199473591
SNP Nexus

SNPshotrs199473591
SNPdbers199473591
MSV3drs199473591
GWAS Ctlgrs199473591
Max Magnitude0
ClinVar
Risk rs199473591(T;T)
Alt rs199473591(T;T)
Reference rs199473591(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.38622708C>A
CLNSRC ClinVar
CLNACC RCV000058538.2,