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rs199473425

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473425(C;C)
Make rs199473425(C;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150951657
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473425
ebirs199473425
HLIrs199473425
Exacrs199473425
Varsomers199473425
Maprs199473425
PheGenIrs199473425
hapmaprs199473425
1000 genomesrs199473425
hgdprs199473425
ensemblrs199473425
gopubmedrs199473425
geneviewrs199473425
scholarrs199473425
googlers199473425
pharmgkbrs199473425
gwascentralrs199473425
openSNPrs199473425
23andMers199473425
23andMe allrs199473425
SNP Nexus

SNPshotrs199473425
SNPdbers199473425
MSV3drs199473425
GWAS Ctlgrs199473425
Max Magnitude0
ClinVar
Risk rs199473425(C;C)
Alt rs199473425(C;C)
Reference rs199473425(T;T)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150648745A>G
CLNSRC ClinVar
CLNACC RCV000057967.2,