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rs794729052

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794729052(A;G)
Make rs794729052(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position41767515
GeneJUP
is asnp
is mentioned by
dbSNPrs794729052
ebirs794729052
HLIrs794729052
Exacrs794729052
Varsomers794729052
Maprs794729052
PheGenIrs794729052
hapmaprs794729052
1000 genomesrs794729052
hgdprs794729052
ensemblrs794729052
gopubmedrs794729052
geneviewrs794729052
scholarrs794729052
googlers794729052
pharmgkbrs794729052
gwascentralrs794729052
openSNPrs794729052
23andMers794729052
23andMe allrs794729052
SNP Nexus

SNPshotrs794729052
SNPdbers794729052
MSV3drs794729052
GWAS Ctlgrs794729052
Max Magnitude0
ClinVar
Risk rs794729052(G;G)
Alt rs794729052(G;G)
Reference rs794729052(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene JUP
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.39923767T>C
CLNSRC
CLNACC RCV000183508.2,