rs12478601, THADA

N. diseases: 5
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 0.851 0.200 2 43494369 intron variant C/T snv 0.61 0.820 0.750 4 2011 2019
Anovulation
CUI: C0003128
Disease: Anovulation
8 0.851 0.200 2 43494369 intron variant C/T snv 0.61 0.010 1.000 1 2015 2015
Anovulatory (finding)
CUI: C0429468
Disease: Anovulatory (finding)
8 0.851 0.200 2 43494369 intron variant C/T snv 0.61 0.010 1.000 1 2015 2015
Hyperandrogenism
CUI: C0206081
Disease: Hyperandrogenism
24 0.851 0.200 2 43494369 intron variant C/T snv 0.61 0.010 1.000 1 2015 2015
Thyroid Gland Follicular Adenoma
CUI: C0151468
Disease: Thyroid Gland Follicular Adenoma
14 0.851 0.200 2 43494369 intron variant C/T snv 0.61 0.010 1.000 1 2015 2015