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rs794728473

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs794728473(-;C)
Make rs794728473(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150946955
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728473
dbSNP (old)rs794728473
ClinGenrs794728473
ebirs794728473
HLIrs794728473
Exacrs794728473
Gnomadrs794728473
Varsomers794728473
Maprs794728473
PheGenIrs794728473
Biobankrs794728473
1000 genomesrs794728473
hgdprs794728473
ensemblrs794728473
gopubmedrs794728473
geneviewrs794728473
scholarrs794728473
googlers794728473
pharmgkbrs794728473
gwascentralrs794728473
openSNPrs794728473
23andMers794728473
23andMe allrs794728473
SNP Nexus

SNPshotrs794728473
SNPdbers794728473
MSV3drs794728473
GWAS Ctlgrs794728473
Max Magnitude0
ClinVar
Risk rs794728473(C;C)
Alt rs794728473(C;C)
Reference Rs794728473(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150644044dupG
CLNSRC
CLNACC RCV000182013.3,