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 0.790 0.200 2 48751020 intron variant A/G snv 0.15 0.900 0.818 11 2011 2019
Adenocarcinoma, Endometrioid
CUI: C1569637
Disease: Adenocarcinoma, Endometrioid
4 0.790 0.200 2 48751020 intron variant A/G snv 0.15 0.010 1.000 1 2012 2012
Anovulation
CUI: C0003128
Disease: Anovulation
8 0.790 0.200 2 48751020 intron variant A/G snv 0.15 0.010 1.000 1 2015 2015
Anovulatory (finding)
CUI: C0429468
Disease: Anovulatory (finding)
8 0.790 0.200 2 48751020 intron variant A/G snv 0.15 0.010 1.000 1 2015 2015
Carcinoma, Endometrioid
CUI: C0206687
Disease: Carcinoma, Endometrioid
12 0.790 0.200 2 48751020 intron variant A/G snv 0.15 0.010 1.000 1 2012 2012
Endometrial Carcinoma
CUI: C0476089
Disease: Endometrial Carcinoma
326 0.790 0.200 2 48751020 intron variant A/G snv 0.15 0.010 1.000 1 2012 2012
Hyperandrogenism
CUI: C0206081
Disease: Hyperandrogenism
24 0.790 0.200 2 48751020 intron variant A/G snv 0.15 0.010 1.000 1 2015 2015
Thyroid Gland Follicular Adenoma
CUI: C0151468
Disease: Thyroid Gland Follicular Adenoma
14 0.790 0.200 2 48751020 intron variant A/G snv 0.15 0.010 1.000 1 2015 2015