rs7605378, FTCDNL1

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.
Osteoporosis
CUI: C0029456
Disease: Osteoporosis
182 0.925 0.120 2 199812203 intron variant A/C snv 0.64 0.830 1.000 3 2011 2015
Werner Syndrome
CUI: C0043119
Disease: Werner Syndrome
71 0.925 0.120 2 199812203 intron variant A/C snv 0.64 0.010 1.000 1 2016 2016