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rs794728401

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728401(A;A)
Make rs794728401(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150947478
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728401
ebirs794728401
HLIrs794728401
Exacrs794728401
Varsomers794728401
Maprs794728401
PheGenIrs794728401
hapmaprs794728401
1000 genomesrs794728401
hgdprs794728401
ensemblrs794728401
gopubmedrs794728401
geneviewrs794728401
scholarrs794728401
googlers794728401
pharmgkbrs794728401
gwascentralrs794728401
openSNPrs794728401
23andMers794728401
23andMe allrs794728401
SNP Nexus

SNPshotrs794728401
SNPdbers794728401
MSV3drs794728401
GWAS Ctlgrs794728401
Max Magnitude0
ClinVar
Risk rs794728401(A;A)
Alt rs794728401(A;A)
Reference rs794728401(G;G)
Significance Pathogenic
Disease not provided Long QT syndrome
Variation info
Gene KCNH2
CLNDBN not provided Long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150644566C>T
CLNSRC
CLNACC RCV000181904.2, RCV000228852.1,