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rs199472935

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199472935(A;A)
Make rs199472935(A;C)
ReferenceGRCh38 38.1/142
Chromosome7
Position150951596
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472935
ebirs199472935
HLIrs199472935
Exacrs199472935
Varsomers199472935
Maprs199472935
PheGenIrs199472935
hapmaprs199472935
1000 genomesrs199472935
hgdprs199472935
ensemblrs199472935
gopubmedrs199472935
geneviewrs199472935
scholarrs199472935
googlers199472935
pharmgkbrs199472935
gwascentralrs199472935
openSNPrs199472935
23andMers199472935
23andMe allrs199472935
SNP Nexus

SNPshotrs199472935
SNPdbers199472935
MSV3drs199472935
GWAS Ctlgrs199472935
Max Magnitude0
ClinVar
Risk rs199472935(A;A)
Alt rs199472935(A;A)
Reference rs199472935(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.150648684G>T
CLNSRC ClinVar
CLNACC RCV000057994.2,