rs121909659, FSHR

N. diseases: 2
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 0.925 0.160 2 48989022 missense variant A/G;T snv 4.0E-05; 4.0E-06 0.700 0
Ovarian Hyperstimulation Syndrome
CUI: C0085083
Disease: Ovarian Hyperstimulation Syndrome
24 0.925 0.160 2 48989022 missense variant A/G;T snv 4.0E-05; 4.0E-06 0.010 1.000 1 2008 2008