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rs199473499

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473499(G;G)
Make rs199473499(G;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150959670
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473499
ebirs199473499
HLIrs199473499
Exacrs199473499
Varsomers199473499
Maprs199473499
PheGenIrs199473499
hapmaprs199473499
1000 genomesrs199473499
hgdprs199473499
ensemblrs199473499
gopubmedrs199473499
geneviewrs199473499
scholarrs199473499
googlers199473499
pharmgkbrs199473499
gwascentralrs199473499
openSNPrs199473499
23andMers199473499
23andMe allrs199473499
SNP Nexus

SNPshotrs199473499
SNPdbers199473499
MSV3drs199473499
GWAS Ctlgrs199473499
Max Magnitude0
ClinVar
Risk rs199473499(G;G)
Alt rs199473499(G;G)
Reference rs199473499(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.150656758A>C
CLNSRC ClinVar
CLNACC RCV000058231.2,