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

rs199472903

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199472903(G;T)
Make rs199472903(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150952604
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472903
ebirs199472903
HLIrs199472903
Exacrs199472903
Varsomers199472903
Maprs199472903
PheGenIrs199472903
hapmaprs199472903
1000 genomesrs199472903
hgdprs199472903
ensemblrs199472903
gopubmedrs199472903
geneviewrs199472903
scholarrs199472903
googlers199472903
pharmgkbrs199472903
gwascentralrs199472903
openSNPrs199472903
23andMers199472903
23andMe allrs199472903
SNP Nexus

SNPshotrs199472903
SNPdbers199472903
MSV3drs199472903
GWAS Ctlgrs199472903
Max Magnitude0
ClinVar
Risk rs199472903(T;T)
Alt rs199472903(T;T)
Reference rs199472903(G;G)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150649692C>A
CLNSRC ClinVar
CLNACC RCV000057899.2,