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rs199473667

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473667(A;G)
Make rs199473667(G;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150951673
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473667
ebirs199473667
HLIrs199473667
Exacrs199473667
Varsomers199473667
Maprs199473667
PheGenIrs199473667
hapmaprs199473667
1000 genomesrs199473667
hgdprs199473667
ensemblrs199473667
gopubmedrs199473667
geneviewrs199473667
scholarrs199473667
googlers199473667
pharmgkbrs199473667
gwascentralrs199473667
openSNPrs199473667
23andMers199473667
23andMe allrs199473667
SNP Nexus

SNPshotrs199473667
SNPdbers199473667
MSV3drs199473667
GWAS Ctlgrs199473667
Max Magnitude0
ClinVar
Risk rs199473667(C,G;C,G)
Alt rs199473667(C,G;C,G)
Reference rs199473667(A;A)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150648761T>C
CLNSRC ClinVar
CLNACC RCV000057964.2,