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rs199473509

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473509(C;T)
Make rs199473509(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150952663
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473509
ebirs199473509
HLIrs199473509
Exacrs199473509
Varsomers199473509
Maprs199473509
PheGenIrs199473509
hapmaprs199473509
1000 genomesrs199473509
hgdprs199473509
ensemblrs199473509
gopubmedrs199473509
geneviewrs199473509
scholarrs199473509
googlers199473509
pharmgkbrs199473509
gwascentralrs199473509
openSNPrs199473509
23andMers199473509
23andMe allrs199473509
SNP Nexus

SNPshotrs199473509
SNPdbers199473509
MSV3drs199473509
GWAS Ctlgrs199473509
Max Magnitude0
ClinVar
Risk rs199473509(T;T)
Alt rs199473509(T;T)
Reference rs199473509(C;C)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150649751G>A
CLNSRC ClinVar
CLNACC RCV000057892.2,