rs10203122, FTCDNL1

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.
Osteoporosis
CUI: C0029456
Disease: Osteoporosis
182 1.000 0.080 2 199831723 intron variant T/C snv 0.16 0.010 1.000 1 2015 2015