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rs782392706

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs782392706(C;G)
Make rs782392706(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position41769480
GeneJUP
is asnp
is mentioned by
dbSNPrs782392706
ebirs782392706
HLIrs782392706
Exacrs782392706
Varsomers782392706
Maprs782392706
PheGenIrs782392706
hapmaprs782392706
1000 genomesrs782392706
hgdprs782392706
ensemblrs782392706
gopubmedrs782392706
geneviewrs782392706
scholarrs782392706
googlers782392706
pharmgkbrs782392706
gwascentralrs782392706
openSNPrs782392706
23andMers782392706
23andMe allrs782392706
SNP Nexus

SNPshotrs782392706
SNPdbers782392706
MSV3drs782392706
GWAS Ctlgrs782392706
Max Magnitude0
ClinVar
Risk rs782392706(G,T;G,T)
Alt rs782392706(G,T;G,T)
Reference rs782392706(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene JUP
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.39925732C>G
CLNSRC
CLNACC RCV000183484.2,