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

rs199473037

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473037(C;C)
Make rs199473037(C;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150974780
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473037
ebirs199473037
HLIrs199473037
Exacrs199473037
Varsomers199473037
Maprs199473037
PheGenIrs199473037
hapmaprs199473037
1000 genomesrs199473037
hgdprs199473037
ensemblrs199473037
gopubmedrs199473037
geneviewrs199473037
scholarrs199473037
googlers199473037
pharmgkbrs199473037
gwascentralrs199473037
openSNPrs199473037
23andMers199473037
23andMe allrs199473037
SNP Nexus

SNPshotrs199473037
SNPdbers199473037
MSV3drs199473037
GWAS Ctlgrs199473037
Max Magnitude0
ClinVar
Risk rs199473037(C;C)
Alt rs199473037(C;C)
Reference rs199473037(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.150671868C>G
CLNSRC ClinVar
CLNACC RCV000058114.2,