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

rs199472897

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199472897(A;G)
Make rs199472897(G;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150952702
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472897
ebirs199472897
HLIrs199472897
Exacrs199472897
Varsomers199472897
Maprs199472897
PheGenIrs199472897
hapmaprs199472897
1000 genomesrs199472897
hgdprs199472897
ensemblrs199472897
gopubmedrs199472897
geneviewrs199472897
scholarrs199472897
googlers199472897
pharmgkbrs199472897
gwascentralrs199472897
openSNPrs199472897
23andMers199472897
23andMe allrs199472897
SNP Nexus

SNPshotrs199472897
SNPdbers199472897
MSV3drs199472897
GWAS Ctlgrs199472897
Max Magnitude0
ClinVar
Risk rs199472897(C,G;C,G)
Alt rs199472897(C,G;C,G)
Reference rs199472897(A;A)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150649790T>C; NC_000007.13:g.150649790T>G
CLNSRC ClinVar
CLNACC RCV000057886.2, RCV000057885.2,