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rs199473013

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473013(A;A)
Make rs199473013(A;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150947692
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473013
ebirs199473013
HLIrs199473013
Exacrs199473013
Varsomers199473013
Maprs199473013
PheGenIrs199473013
hapmaprs199473013
1000 genomesrs199473013
hgdprs199473013
ensemblrs199473013
gopubmedrs199473013
geneviewrs199473013
scholarrs199473013
googlers199473013
pharmgkbrs199473013
gwascentralrs199473013
openSNPrs199473013
23andMers199473013
23andMe allrs199473013
SNP Nexus

SNPshotrs199473013
SNPdbers199473013
MSV3drs199473013
GWAS Ctlgrs199473013
Max Magnitude0
ClinVar
Risk rs199473013(A;A)
Alt rs199473013(A;A)
Reference rs199473013(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.150644780C>T
CLNSRC ClinVar
CLNACC RCV000058174.2,