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rs199473007

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473007(A;C)
Make rs199473007(C;C)
ReferenceGRCh38 38.1/142
Chromosome7
Position150948867
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473007
ebirs199473007
HLIrs199473007
Exacrs199473007
Varsomers199473007
Maprs199473007
PheGenIrs199473007
hapmaprs199473007
1000 genomesrs199473007
hgdprs199473007
ensemblrs199473007
gopubmedrs199473007
geneviewrs199473007
scholarrs199473007
googlers199473007
pharmgkbrs199473007
gwascentralrs199473007
openSNPrs199473007
23andMers199473007
23andMe allrs199473007
SNP Nexus

SNPshotrs199473007
SNPdbers199473007
MSV3drs199473007
GWAS Ctlgrs199473007
Max Magnitude0
ClinVar
Risk rs199473007(C;C)
Alt rs199473007(C;C)
Reference rs199473007(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.150645955T>G
CLNSRC ClinVar
CLNACC RCV000058139.2,