rs2269336, COL1A1

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.
Severe myopia
CUI: C0271183
Disease: Severe myopia
116 1.000 0.040 17 50202995 intron variant G/A;C snv 0.030 0.667 3 2007 2011