rs9694676, LRP12

N. diseases: 2
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 0.925 0.080 8 104588948 5 prime UTR variant A/G snv 8.6E-02 0.20 0.010 1.000 1 2016 2016
Ganglioglioma
CUI: C0206716
Disease: Ganglioglioma
7 0.925 0.080 8 104588948 5 prime UTR variant A/G snv 8.6E-02 0.20 0.010 1.000 1 2016 2016