rs10033900, CFI

N. diseases: 7
Disease: Myopia ×
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 0.807 0.040 4 109737911 intron variant T/C snv 0.54 0.010 1.000 1 2012 2012