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

rs199473034

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473034(G;T)
Make rs199473034(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150945415
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473034
ebirs199473034
HLIrs199473034
Exacrs199473034
Varsomers199473034
Maprs199473034
PheGenIrs199473034
hapmaprs199473034
1000 genomesrs199473034
hgdprs199473034
ensemblrs199473034
gopubmedrs199473034
geneviewrs199473034
scholarrs199473034
googlers199473034
pharmgkbrs199473034
gwascentralrs199473034
openSNPrs199473034
23andMers199473034
23andMe allrs199473034
SNP Nexus

SNPshotrs199473034
SNPdbers199473034
MSV3drs199473034
GWAS Ctlgrs199473034
Max Magnitude0
ClinVar
Risk rs199473034(A,T;A,T)
Alt rs199473034(A,T;A,T)
Reference rs199473034(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.150642503C>T
CLNSRC ClinVar
CLNACC RCV000058224.2,