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

rs199472919

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199472919(A;A)
Make rs199472919(A;C)
ReferenceGRCh38 38.1/142
Chromosome7
Position150951720
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472919
ebirs199472919
HLIrs199472919
Exacrs199472919
Varsomers199472919
Maprs199472919
PheGenIrs199472919
hapmaprs199472919
1000 genomesrs199472919
hgdprs199472919
ensemblrs199472919
gopubmedrs199472919
geneviewrs199472919
scholarrs199472919
googlers199472919
pharmgkbrs199472919
gwascentralrs199472919
openSNPrs199472919
23andMers199472919
23andMe allrs199472919
SNP Nexus

SNPshotrs199472919
SNPdbers199472919
MSV3drs199472919
GWAS Ctlgrs199472919
Max Magnitude0
ClinVar
Risk rs199472919(A;A)
Alt rs199472919(A;A)
Reference rs199472919(C;C)
Significance Pathogenic
Disease Congenital long QT syndrome not provided
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome not provided
Reversed 1
HGVS NC_000007.13:g.150648808G>T
CLNSRC ClinVar
CLNACC RCV000057936.2, RCV000182025.2,