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

rs199472907

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199472907(A;G)
Make rs199472907(G;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150952558
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472907
ebirs199472907
HLIrs199472907
Exacrs199472907
Varsomers199472907
Maprs199472907
PheGenIrs199472907
hapmaprs199472907
1000 genomesrs199472907
hgdprs199472907
ensemblrs199472907
gopubmedrs199472907
geneviewrs199472907
scholarrs199472907
googlers199472907
pharmgkbrs199472907
gwascentralrs199472907
openSNPrs199472907
23andMers199472907
23andMe allrs199472907
SNP Nexus

SNPshotrs199472907
SNPdbers199472907
MSV3drs199472907
GWAS Ctlgrs199472907
Max Magnitude0
ClinVar
Risk rs199472907(G;G)
Alt rs199472907(G;G)
Reference rs199472907(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.150649646T>C
CLNSRC ClinVar
CLNACC RCV000057907.2,