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

rs199473540

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473540(A;A)
Make rs199473540(A;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150947761
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473540
ebirs199473540
HLIrs199473540
Exacrs199473540
Varsomers199473540
Maprs199473540
PheGenIrs199473540
hapmaprs199473540
1000 genomesrs199473540
hgdprs199473540
ensemblrs199473540
gopubmedrs199473540
geneviewrs199473540
scholarrs199473540
googlers199473540
pharmgkbrs199473540
gwascentralrs199473540
openSNPrs199473540
23andMers199473540
23andMe allrs199473540
SNP Nexus

SNPshotrs199473540
SNPdbers199473540
MSV3drs199473540
GWAS Ctlgrs199473540
Max Magnitude0
ClinVar
Risk rs199473540(A;A)
Alt rs199473540(A;A)
Reference rs199473540(G;G)
Significance Pathogenic
Disease Congenital long QT syndrome not specified
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome not specified
Reversed 1
HGVS NC_000007.13:g.150644849C>T
CLNSRC ClinVar
CLNACC RCV000058166.2, RCV000181897.2,