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rs199473021

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473021(C;T)
Make rs199473021(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150947383
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473021
ebirs199473021
HLIrs199473021
Exacrs199473021
Varsomers199473021
Maprs199473021
PheGenIrs199473021
hapmaprs199473021
1000 genomesrs199473021
hgdprs199473021
ensemblrs199473021
gopubmedrs199473021
geneviewrs199473021
scholarrs199473021
googlers199473021
pharmgkbrs199473021
gwascentralrs199473021
openSNPrs199473021
23andMers199473021
23andMe allrs199473021
SNP Nexus

SNPshotrs199473021
SNPdbers199473021
MSV3drs199473021
GWAS Ctlgrs199473021
Max Magnitude0
ClinVar
Risk rs199473021(T;T)
Alt rs199473021(T;T)
Reference rs199473021(C;C)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150644471G>A
CLNSRC ClinVar
CLNACC RCV000058195.2,