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rs794728459

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728459(-;-)
Make rs794728459(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150947665
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728459
dbSNP (classic)rs794728459
ClinGenrs794728459
ebirs794728459
HLIrs794728459
Exacrs794728459
Gnomadrs794728459
Varsomers794728459
LitVarrs794728459
Maprs794728459
PheGenIrs794728459
Biobankrs794728459
1000 genomesrs794728459
hgdprs794728459
ensemblrs794728459
geneviewrs794728459
scholarrs794728459
googlers794728459
pharmgkbrs794728459
gwascentralrs794728459
openSNPrs794728459
23andMers794728459
SNPshotrs794728459
SNPdbers794728459
MSV3drs794728459
GWAS Ctlgrs794728459
Max Magnitude0
ClinVar
Risk rs794728459(-;-)
Alt rs794728459(-;-)
Reference Rs794728459(G;G)
Significance Pathogenic
Disease Cardiac arrhythmia
Variation info
Gene KCNH2
CLNDBN Cardiac arrhythmia
Reversed 1
HGVS NC_000007.13:g.150644753delC
CLNSRC
CLNACC RCV000181997.1,