rs4385527, AOPEP

N. diseases: 6
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 0.827 0.280 9 94886305 intron variant G/A snv 0.31 0.720 1.000 3 2012 2015
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.827 0.280 9 94886305 intron variant G/A snv 0.31 0.700 1.000 1 2018 2018
Anovulation
CUI: C0003128
Disease: Anovulation
8 0.827 0.280 9 94886305 intron variant G/A snv 0.31 0.010 1.000 1 2015 2015
Anovulatory (finding)
CUI: C0429468
Disease: Anovulatory (finding)
8 0.827 0.280 9 94886305 intron variant G/A snv 0.31 0.010 1.000 1 2015 2015
Hyperandrogenism
CUI: C0206081
Disease: Hyperandrogenism
24 0.827 0.280 9 94886305 intron variant G/A snv 0.31 0.010 1.000 1 2015 2015
Thyroid Gland Follicular Adenoma
CUI: C0151468
Disease: Thyroid Gland Follicular Adenoma
14 0.827 0.280 9 94886305 intron variant G/A snv 0.31 0.010 1.000 1 2015 2015