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rs199472887

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199472887(A;A)
Make rs199472887(A;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150957452
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472887
ebirs199472887
HLIrs199472887
Exacrs199472887
Varsomers199472887
Maprs199472887
PheGenIrs199472887
hapmaprs199472887
1000 genomesrs199472887
hgdprs199472887
ensemblrs199472887
gopubmedrs199472887
geneviewrs199472887
scholarrs199472887
googlers199472887
pharmgkbrs199472887
gwascentralrs199472887
openSNPrs199472887
23andMers199472887
23andMe allrs199472887
SNP Nexus

SNPshotrs199472887
SNPdbers199472887
MSV3drs199472887
GWAS Ctlgrs199472887
Max Magnitude0
ClinVar
Risk rs199472887(A;A)
Alt rs199472887(A;A)
Reference rs199472887(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.150654540C>T
CLNSRC ClinVar
CLNACC RCV000058280.2,