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

rs199472827

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199472827(G;T)
Make rs199472827(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150974941
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472827
ebirs199472827
HLIrs199472827
Exacrs199472827
Varsomers199472827
Maprs199472827
PheGenIrs199472827
hapmaprs199472827
1000 genomesrs199472827
hgdprs199472827
ensemblrs199472827
gopubmedrs199472827
geneviewrs199472827
scholarrs199472827
googlers199472827
pharmgkbrs199472827
gwascentralrs199472827
openSNPrs199472827
23andMers199472827
23andMe allrs199472827
SNP Nexus

SNPshotrs199472827
SNPdbers199472827
MSV3drs199472827
GWAS Ctlgrs199472827
Max Magnitude0
ClinVar
Risk rs199472827(T;T)
Alt rs199472827(T;T)
Reference rs199472827(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.150672029C>A
CLNSRC ClinVar
CLNACC RCV000058257.2,