rs1635529, COL2A1

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.
Myopia
CUI: C0027092
Disease: Myopia
167 0.925 0.040 12 48001319 intron variant T/G snv 0.78 0.010 1.000 1 2012 2012
Severe myopia
CUI: C0271183
Disease: Severe myopia
116 0.925 0.040 12 48001319 intron variant T/G snv 0.78 0.010 1 2012 2012