rs121965049, OAT

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.
Gyrate Atrophy
CUI: C0018425
Disease: Gyrate Atrophy
35 1.000 0.080 10 124401785 missense variant G/A snv 0.700 1.000 7 1988 2013
Hyperornithinemia
CUI: C0599035
Disease: Hyperornithinemia
65 1.000 0.080 10 124401785 missense variant G/A snv 0.700 0