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rs199472859

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199472859(C;C)
Make rs199472859(C;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150959722
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472859
ebirs199472859
HLIrs199472859
Exacrs199472859
Varsomers199472859
Maprs199472859
PheGenIrs199472859
hapmaprs199472859
1000 genomesrs199472859
hgdprs199472859
ensemblrs199472859
gopubmedrs199472859
geneviewrs199472859
scholarrs199472859
googlers199472859
pharmgkbrs199472859
gwascentralrs199472859
openSNPrs199472859
23andMers199472859
23andMe allrs199472859
SNP Nexus

SNPshotrs199472859
SNPdbers199472859
MSV3drs199472859
GWAS Ctlgrs199472859
Max Magnitude0
ClinVar
Risk rs199472859(C;C)
Alt rs199472859(C;C)
Reference rs199472859(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.150656810A>G
CLNSRC ClinVar
CLNACC RCV000058211.2,