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rs794728437

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TAC;TAC) 0 common in clinvar
Make rs794728437(-;-)
Make rs794728437(-;TAC)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150952557
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728437
dbSNP (classic)rs794728437
ClinGenrs794728437
ebirs794728437
HLIrs794728437
Exacrs794728437
Gnomadrs794728437
Varsomers794728437
LitVarrs794728437
Maprs794728437
PheGenIrs794728437
Biobankrs794728437
1000 genomesrs794728437
hgdprs794728437
ensemblrs794728437
geneviewrs794728437
scholarrs794728437
googlers794728437
pharmgkbrs794728437
gwascentralrs794728437
openSNPrs794728437
23andMers794728437
SNPshotrs794728437
SNPdbers794728437
MSV3drs794728437
GWAS Ctlgrs794728437
Max Magnitude0
ClinVar
Risk rs794728437(-;-)
Alt rs794728437(-;-)
Reference Rs794728437(TAC;TAC)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150649645_150649647delGTA
CLNSRC
CLNACC RCV000181975.2,