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

rs199472885

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199472885(C;T)
Make rs199472885(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150957485
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472885
ebirs199472885
HLIrs199472885
Exacrs199472885
Varsomers199472885
Maprs199472885
PheGenIrs199472885
hapmaprs199472885
1000 genomesrs199472885
hgdprs199472885
ensemblrs199472885
gopubmedrs199472885
geneviewrs199472885
scholarrs199472885
googlers199472885
pharmgkbrs199472885
gwascentralrs199472885
openSNPrs199472885
23andMers199472885
23andMe allrs199472885
SNP Nexus

SNPshotrs199472885
SNPdbers199472885
MSV3drs199472885
GWAS Ctlgrs199472885
Max Magnitude0
ClinVar
Risk rs199472885(T;T)
Alt rs199472885(T;T)
Reference rs199472885(C;C)
Significance Other
Disease Congenital long QT syndrome Long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome Long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150654573G>A
CLNSRC ClinVar
CLNACC RCV000058276.2, RCV000171561.2,