rs10887265, RGR

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
CUI: C0027092
Disease: Myopia
167 1.000 0.040 10 84255817 intron variant G/C snv 0.48 0.700 1.000 1 2016 2016