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rs199473020

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473020(A;A)
Make rs199473020(A;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150947385
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473020
ebirs199473020
HLIrs199473020
Exacrs199473020
Varsomers199473020
Maprs199473020
PheGenIrs199473020
hapmaprs199473020
1000 genomesrs199473020
hgdprs199473020
ensemblrs199473020
gopubmedrs199473020
geneviewrs199473020
scholarrs199473020
googlers199473020
pharmgkbrs199473020
gwascentralrs199473020
openSNPrs199473020
23andMers199473020
23andMe allrs199473020
SNP Nexus

SNPshotrs199473020
SNPdbers199473020
MSV3drs199473020
GWAS Ctlgrs199473020
Max Magnitude0
ClinVar
Risk rs199473020(A,T;A,T)
Alt rs199473020(A,T;A,T)
Reference rs199473020(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.150644473C>T
CLNSRC ClinVar
CLNACC RCV000058194.2,