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rs794728403

From SNPedia

Orientationminus
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
ebirs794728403
HLIrs794728403
Exacrs794728403
Varsomers794728403
Maprs794728403
PheGenIrs794728403
hapmaprs794728403
1000 genomesrs794728403
hgdprs794728403
ensemblrs794728403
gopubmedrs794728403
geneviewrs794728403
scholarrs794728403
googlers794728403
pharmgkbrs794728403
gwascentralrs794728403
openSNPrs794728403
23andMers794728403
23andMe allrs794728403
SNP Nexus

SNPshotrs794728403
SNPdbers794728403
MSV3drs794728403
GWAS Ctlgrs794728403
Max Magnitude0
ClinVar
Risk rs794728403(T;T)
Alt rs794728403(T;T)
Reference rs794728403(C;C)
Significance Pathogenic
Disease Cardiac arrhythmia Long QT syndrome not provided
Variation info
Gene KCNH2
CLNDBN Cardiac arrhythmia Long QT syndrome not provided
Reversed 1
HGVS NC_000007.13:g.150644528G>A
CLNSRC
CLNACC RCV000181907.1, RCV000204945.1, RCV000223784.1,