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

rs199472976

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199472976(C;T)
Make rs199472976(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150951120
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472976
ebirs199472976
HLIrs199472976
Exacrs199472976
Varsomers199472976
Maprs199472976
PheGenIrs199472976
hapmaprs199472976
1000 genomesrs199472976
hgdprs199472976
ensemblrs199472976
gopubmedrs199472976
geneviewrs199472976
scholarrs199472976
googlers199472976
pharmgkbrs199472976
gwascentralrs199472976
openSNPrs199472976
23andMers199472976
23andMe allrs199472976
SNP Nexus

SNPshotrs199472976
SNPdbers199472976
MSV3drs199472976
GWAS Ctlgrs199472976
Max Magnitude0
ClinVar
Risk rs199472976(T;T)
Alt rs199472976(T;T)
Reference rs199472976(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.150648208G>A
CLNSRC ClinVar
CLNACC RCV000058066.2,