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rs199473525

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473525(C;T)
Make rs199473525(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150951529
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473525
ebirs199473525
HLIrs199473525
Exacrs199473525
Varsomers199473525
Maprs199473525
PheGenIrs199473525
hapmaprs199473525
1000 genomesrs199473525
hgdprs199473525
ensemblrs199473525
gopubmedrs199473525
geneviewrs199473525
scholarrs199473525
googlers199473525
pharmgkbrs199473525
gwascentralrs199473525
openSNPrs199473525
23andMers199473525
23andMe allrs199473525
SNP Nexus

SNPshotrs199473525
SNPdbers199473525
MSV3drs199473525
GWAS Ctlgrs199473525
Max Magnitude0
ClinVar
Risk rs199473525(T;T)
Alt rs199473525(T;T)
Reference rs199473525(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.150648617G>A
CLNSRC ClinVar
CLNACC RCV000058019.2,