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rs794728403

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728403(C;T)
Make rs794728403(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150947440
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728403
dbSNP (classic)rs794728403
ClinGenrs794728403
ebirs794728403
HLIrs794728403
Exacrs794728403
Gnomadrs794728403
Varsomers794728403
LitVarrs794728403
Maprs794728403
PheGenIrs794728403
Biobankrs794728403
1000 genomesrs794728403
hgdprs794728403
ensemblrs794728403
geneviewrs794728403
scholarrs794728403
googlers794728403
pharmgkbrs794728403
gwascentralrs794728403
openSNPrs794728403
23andMers794728403
SNPshotrs794728403
SNPdbers794728403
MSV3drs794728403
GWAS Ctlgrs794728403
Max Magnitude0
ClinVar
Risk rs794728403(T;T)
Alt rs794728403(T;T)
Reference Rs794728403(C;C)
Significance Pathogenic
Disease Long QT syndrome not provided
Variation info
Gene KCNH2
CLNDBN Long QT syndrome not provided
Reversed 1
HGVS NC_000007.13:g.150644528G>A
CLNSRC
CLNACC RCV000204945.2, RCV000223784.2,