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.
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
363 0.882 0.120 11 30204981 intron variant G/A snv 0.11 0.710 1.000 2 2015 2015
Age at menarche
CUI: C1314691
Disease: Age at menarche
591 0.882 0.120 11 30204981 intron variant G/A snv 0.11 0.700 1.000 1 2019 2019
Age at menopause
CUI: C1629609
Disease: Age at menopause
209 0.882 0.120 11 30204981 intron variant G/A snv 0.11 0.700 1.000 1 2015 2015
Luteinizing hormone measurement
CUI: C0202123
Disease: Luteinizing hormone measurement
5 0.882 0.120 11 30204981 intron variant G/A snv 0.11 0.700 1.000 1 2015 2015
Menorrhagia
CUI: C0025323
Disease: Menorrhagia
6 0.882 0.120 11 30204981 intron variant G/A snv 0.11 0.700 1.000 1 2019 2019
Plexiform leiomyoma
CUI: C2242776
Disease: Plexiform leiomyoma
103 0.882 0.120 11 30204981 intron variant G/A snv 0.11 0.700 1.000 1 2019 2019
Uterine Fibroids
CUI: C0042133
Disease: Uterine Fibroids
154 0.882 0.120 11 30204981 intron variant G/A snv 0.11 0.700 1.000 1 2019 2019
Endometriosis
CUI: C0014175
Disease: Endometriosis
274 0.882 0.120 11 30204981 intron variant G/A snv 0.11 0.010 1.000 1 2017 2017