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

rs199472834

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199472834(A;A)
Make rs199472834(A;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150974924
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472834
ebirs199472834
HLIrs199472834
Exacrs199472834
Varsomers199472834
Maprs199472834
PheGenIrs199472834
hapmaprs199472834
1000 genomesrs199472834
hgdprs199472834
ensemblrs199472834
gopubmedrs199472834
geneviewrs199472834
scholarrs199472834
googlers199472834
pharmgkbrs199472834
gwascentralrs199472834
openSNPrs199472834
23andMers199472834
23andMe allrs199472834
SNP Nexus

SNPshotrs199472834
SNPdbers199472834
MSV3drs199472834
GWAS Ctlgrs199472834
Max Magnitude0
ClinVar
Risk rs199472834(A;A)
Alt rs199472834(A;A)
Reference rs199472834(G;G)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150672012C>T
CLNSRC ClinVar
CLNACC RCV000058278.2,