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rs794729032

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794729032(C;C)
Make rs794729032(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position41769480
GeneJUP
is asnp
is mentioned by
dbSNPrs794729032
ebirs794729032
HLIrs794729032
Exacrs794729032
Varsomers794729032
Maprs794729032
PheGenIrs794729032
hapmaprs794729032
1000 genomesrs794729032
hgdprs794729032
ensemblrs794729032
gopubmedrs794729032
geneviewrs794729032
scholarrs794729032
googlers794729032
pharmgkbrs794729032
gwascentralrs794729032
openSNPrs794729032
23andMers794729032
23andMe allrs794729032
SNP Nexus

SNPshotrs794729032
SNPdbers794729032
MSV3drs794729032
GWAS Ctlgrs794729032
Max Magnitude0
ClinVar
Risk rs794729032(C;C)
Alt rs794729032(C;C)
Reference rs794729032(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene JUP
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.39925732C>G
CLNSRC
CLNACC RCV000183484.2,