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rs199473496

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473496(A;G)
Make rs199473496(G;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150974732
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473496
ebirs199473496
HLIrs199473496
Exacrs199473496
Varsomers199473496
Maprs199473496
PheGenIrs199473496
hapmaprs199473496
1000 genomesrs199473496
hgdprs199473496
ensemblrs199473496
gopubmedrs199473496
geneviewrs199473496
scholarrs199473496
googlers199473496
pharmgkbrs199473496
gwascentralrs199473496
openSNPrs199473496
23andMers199473496
23andMe allrs199473496
SNP Nexus

SNPshotrs199473496
SNPdbers199473496
MSV3drs199473496
GWAS Ctlgrs199473496
Max Magnitude0
ClinVar
Risk rs199473496(G;G)
Alt rs199473496(G;G)
Reference rs199473496(A;A)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150671820T>C
CLNSRC ClinVar
CLNACC RCV000058173.2,