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rs199472959

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199472959(G;G)
Make rs199472959(G;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150951502
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472959
ebirs199472959
HLIrs199472959
Exacrs199472959
Varsomers199472959
Maprs199472959
PheGenIrs199472959
hapmaprs199472959
1000 genomesrs199472959
hgdprs199472959
ensemblrs199472959
gopubmedrs199472959
geneviewrs199472959
scholarrs199472959
googlers199472959
pharmgkbrs199472959
gwascentralrs199472959
openSNPrs199472959
23andMers199472959
23andMe allrs199472959
SNP Nexus

SNPshotrs199472959
SNPdbers199472959
MSV3drs199472959
GWAS Ctlgrs199472959
Max Magnitude0
ClinVar
Risk rs199472959(G;G)
Alt rs199472959(G;G)
Reference rs199472959(T;T)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150648590A>C
CLNSRC ClinVar
CLNACC RCV000058039.2,