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rs794728458

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs794728458(-;G)
Make rs794728458(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150947785
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728458
dbSNP (old)rs794728458
ClinGenrs794728458
ebirs794728458
HLIrs794728458
Exacrs794728458
Varsomers794728458
Maprs794728458
PheGenIrs794728458
Biobankrs794728458
1000 genomesrs794728458
hgdprs794728458
ensemblrs794728458
gopubmedrs794728458
geneviewrs794728458
scholarrs794728458
googlers794728458
pharmgkbrs794728458
gwascentralrs794728458
openSNPrs794728458
23andMers794728458
23andMe allrs794728458
SNP Nexus

SNPshotrs794728458
SNPdbers794728458
MSV3drs794728458
GWAS Ctlgrs794728458
Max Magnitude0
ClinVar
Risk rs794728458(G;G)
Alt rs794728458(G;G)
Reference Rs794728458(-;-)
Significance Pathogenic
Disease not specified
Variation info
Gene KCNH2
CLNDBN not specified
Reversed 1
HGVS NC_000007.13:g.150644874dupC
CLNSRC
CLNACC RCV000181996.2,