rs1057518927, OAT

N. diseases: 4
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.
Abnormal choroid morphology
CUI: C4025836
Disease: Abnormal choroid morphology
1 0.925 0.080 10 124402952 missense variant T/C snv 0.700 0
Optic Atrophy
CUI: C0029124
Disease: Optic Atrophy
51 0.925 0.080 10 124402952 missense variant T/C snv 0.700 0
Pain
CUI: C0030193
Disease: Pain
196 0.925 0.080 10 124402952 missense variant T/C snv 0.700 0
Visual field defects
CUI: C3887875
Disease: Visual field defects
1 0.925 0.080 10 124402952 missense variant T/C snv 0.700 0