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rs199473028

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473028(C;T)
Make rs199473028(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150946983
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473028
ebirs199473028
HLIrs199473028
Exacrs199473028
Varsomers199473028
Maprs199473028
PheGenIrs199473028
hapmaprs199473028
1000 genomesrs199473028
hgdprs199473028
ensemblrs199473028
gopubmedrs199473028
geneviewrs199473028
scholarrs199473028
googlers199473028
pharmgkbrs199473028
gwascentralrs199473028
openSNPrs199473028
23andMers199473028
23andMe allrs199473028
SNP Nexus

SNPshotrs199473028
SNPdbers199473028
MSV3drs199473028
GWAS Ctlgrs199473028
Max Magnitude0
ClinVar
Risk rs199473028(T;T)
Alt rs199473028(T;T)
Reference rs199473028(C;C)
Significance Pathogenic
Disease Congenital long QT syndrome Long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome Long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150644071G>A
CLNSRC ClinVar University of Washington
CLNACC RCV000058210.2, RCV000148530.1,