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rs199473429

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473429(G;T)
Make rs199473429(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150951642
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473429
ebirs199473429
HLIrs199473429
Exacrs199473429
Varsomers199473429
Maprs199473429
PheGenIrs199473429
hapmaprs199473429
1000 genomesrs199473429
hgdprs199473429
ensemblrs199473429
gopubmedrs199473429
geneviewrs199473429
scholarrs199473429
googlers199473429
pharmgkbrs199473429
gwascentralrs199473429
openSNPrs199473429
23andMers199473429
23andMe allrs199473429
SNP Nexus

SNPshotrs199473429
SNPdbers199473429
MSV3drs199473429
GWAS Ctlgrs199473429
Max Magnitude0
ClinVar
Risk rs199473429(T;T)
Alt rs199473429(T;T)
Reference rs199473429(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.150648730C>A
CLNSRC ClinVar
CLNACC RCV000057977.2,