rs386833511, FSHR

N. diseases: 3
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.
Gonadal Dysgenesis, 46,XX
CUI: C0949595
Disease: Gonadal Dysgenesis, 46,XX
11 0.882 0.200 2 48963097 missense variant G/A snv 0.700 0
Ovarian Hyperstimulation Syndrome
CUI: C0085083
Disease: Ovarian Hyperstimulation Syndrome
24 0.882 0.200 2 48963097 missense variant G/A snv 0.010 1.000 1 2015 2015
Primary physiologic amenorrhea
CUI: C0232939
Disease: Primary physiologic amenorrhea
10 0.882 0.200 2 48963097 missense variant G/A snv 0.010 1.000 1 2010 2010