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

rs199472915

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199472915(C;T)
Make rs199472915(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150951802
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472915
ebirs199472915
HLIrs199472915
Exacrs199472915
Varsomers199472915
Maprs199472915
PheGenIrs199472915
hapmaprs199472915
1000 genomesrs199472915
hgdprs199472915
ensemblrs199472915
gopubmedrs199472915
geneviewrs199472915
scholarrs199472915
googlers199472915
pharmgkbrs199472915
gwascentralrs199472915
openSNPrs199472915
23andMers199472915
23andMe allrs199472915
SNP Nexus

SNPshotrs199472915
SNPdbers199472915
MSV3drs199472915
GWAS Ctlgrs199472915
Max Magnitude0
ClinVar
Risk rs199472915(T;T)
Alt rs199472915(T;T)
Reference rs199472915(C;C)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150648890G>A
CLNSRC ClinVar
CLNACC RCV000057927.2,