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rs794728436

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs794728436(-;C)
Make rs794728436(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150952662
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728436
dbSNP (old)rs794728436
ClinGenrs794728436
ebirs794728436
HLIrs794728436
Exacrs794728436
Gnomadrs794728436
Varsomers794728436
Maprs794728436
PheGenIrs794728436
Biobankrs794728436
1000 genomesrs794728436
hgdprs794728436
ensemblrs794728436
gopubmedrs794728436
geneviewrs794728436
scholarrs794728436
googlers794728436
pharmgkbrs794728436
gwascentralrs794728436
openSNPrs794728436
23andMers794728436
23andMe allrs794728436
SNP Nexus

SNPshotrs794728436
SNPdbers794728436
MSV3drs794728436
GWAS Ctlgrs794728436
Max Magnitude0
ClinVar
Risk rs794728436(C;C)
Alt rs794728436(C;C)
Reference Rs794728436(-;-)
Significance Pathogenic
Disease Cardiac arrhythmia
Variation info
Gene KCNH2
CLNDBN Cardiac arrhythmia
Reversed 1
HGVS NC_000007.13:g.150649751dupG
CLNSRC
CLNACC RCV000181974.1,