rs669676, COL8A1

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.
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 1.000 0.040 3 99730008 intron variant A/G snv 0.45 0.010 1.000 1 2016 2016
Myopia
CUI: C0027092
Disease: Myopia
167 1.000 0.040 3 99730008 intron variant A/G snv 0.45 0.010 1.000 1 2016 2016