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rs199473003

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473003(C;T)
Make rs199473003(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150948945
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473003
ebirs199473003
HLIrs199473003
Exacrs199473003
Varsomers199473003
Maprs199473003
PheGenIrs199473003
hapmaprs199473003
1000 genomesrs199473003
hgdprs199473003
ensemblrs199473003
gopubmedrs199473003
geneviewrs199473003
scholarrs199473003
googlers199473003
pharmgkbrs199473003
gwascentralrs199473003
openSNPrs199473003
23andMers199473003
23andMe allrs199473003
SNP Nexus

SNPshotrs199473003
SNPdbers199473003
MSV3drs199473003
GWAS Ctlgrs199473003
Max Magnitude0
ClinVar
Risk rs199473003(T;T)
Alt rs199473003(T;T)
Reference rs199473003(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.150646033G>A
CLNSRC ClinVar
CLNACC RCV000058128.2,