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rs199473535

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473535(C;C)
Make rs199473535(C;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150950202
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473535
ebirs199473535
HLIrs199473535
Exacrs199473535
Varsomers199473535
Maprs199473535
PheGenIrs199473535
hapmaprs199473535
1000 genomesrs199473535
hgdprs199473535
ensemblrs199473535
gopubmedrs199473535
geneviewrs199473535
scholarrs199473535
googlers199473535
pharmgkbrs199473535
gwascentralrs199473535
openSNPrs199473535
23andMers199473535
23andMe allrs199473535
SNP Nexus

SNPshotrs199473535
SNPdbers199473535
MSV3drs199473535
GWAS Ctlgrs199473535
Max Magnitude0
ClinVar
Risk rs199473535(C;C)
Alt rs199473535(C;C)
Reference rs199473535(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.150647290C>G
CLNSRC ClinVar
CLNACC RCV000058112.2,