rs113985657, EXOC2

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.
Tonometry
CUI: C0040420
Disease: Tonometry
573 1.000 0.040 6 597203 intron variant C/T snv 0.14 0.700 1.000 3 2018 2018
Glaucoma
CUI: C0017601
Disease: Glaucoma
198 1.000 0.040 6 597203 intron variant C/T snv 0.14 0.700 1.000 1 2018 2018