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rs794728474

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs794728474(-;C)
Make rs794728474(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150945374
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728474
dbSNP (old)rs794728474
ClinGenrs794728474
ebirs794728474
HLIrs794728474
Exacrs794728474
Varsomers794728474
Maprs794728474
PheGenIrs794728474
Biobankrs794728474
1000 genomesrs794728474
hgdprs794728474
ensemblrs794728474
gopubmedrs794728474
geneviewrs794728474
scholarrs794728474
googlers794728474
pharmgkbrs794728474
gwascentralrs794728474
openSNPrs794728474
23andMers794728474
23andMe allrs794728474
SNP Nexus

SNPshotrs794728474
SNPdbers794728474
MSV3drs794728474
GWAS Ctlgrs794728474
Max Magnitude0
ClinVar
Risk rs794728474(C;C)
Alt rs794728474(C;C)
Reference Rs794728474(-;-)
Significance Pathogenic
Disease not specified
Variation info
Gene KCNH2
CLNDBN not specified
Reversed 1
HGVS NC_000007.13:g.150642463dupG
CLNSRC
CLNACC RCV000182014.2,