rs923375, ASPA;SPATA22

N. diseases: 1
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.
Myopia, Degenerative
CUI: C0154778
Disease: Myopia, Degenerative
58 1.000 0.040 17 3489774 intron variant T/C;G snv 0.700 1.000 1 2012 2012