rs2249492, COL1A1

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.
Myalgia
CUI: C0231528
Disease: Myalgia
22 1.000 0.040 17 50185660 intron variant C/G;T snv 0.59 0.010 1.000 1 2018 2018
Pelvic Organ Prolapse
CUI: C0877015
Disease: Pelvic Organ Prolapse
49 1.000 0.040 17 50185660 intron variant C/G;T snv 0.59 0.010 1 2020 2020