rs58073046, ARHGEF12

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.
Glaucoma
CUI: C0017601
Disease: Glaucoma
198 1.000 0.040 11 120377784 intron variant A/G snv 8.7E-02 0.700 1.000 1 2018 2018
Tonometry
CUI: C0040420
Disease: Tonometry
573 1.000 0.040 11 120377784 intron variant A/G snv 8.7E-02 0.700 1.000 1 2017 2017