rs6166, FSHR

N. diseases: 17
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 0.708 0.240 2 48962782 missense variant C/T snv 0.57 0.57 0.090 0.667 9 2001 2017
Male infertility
CUI: C0021364
Disease: Male infertility
146 0.708 0.240 2 48962782 missense variant C/T snv 0.57 0.57 0.060 0.500 6 2011 2017
Endometriosis
CUI: C0014175
Disease: Endometriosis
274 0.708 0.240 2 48962782 missense variant C/T snv 0.57 0.57 0.040 1.000 4 2011 2018
Ovarian Failure, Premature
CUI: C0085215
Disease: Ovarian Failure, Premature
115 0.708 0.240 2 48962782 missense variant C/T snv 0.57 0.57 0.040 1.000 4 1998 2019
Ovarian Hyperstimulation Syndrome
CUI: C0085083
Disease: Ovarian Hyperstimulation Syndrome
24 0.708 0.240 2 48962782 missense variant C/T snv 0.57 0.57 0.030 0.667 3 2004 2009
Premature Menopause
CUI: C0025322
Disease: Premature Menopause
90 0.708 0.240 2 48962782 missense variant C/T snv 0.57 0.57 0.030 1.000 3 1998 2011
Carcinoma, Ovarian Epithelial
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
327 0.708 0.240 2 48962782 missense variant C/T snv 0.57 0.57 0.020 1.000 2 2009 2014
Malignant neoplasm of ovary
CUI: C1140680
Disease: Malignant neoplasm of ovary
315 0.708 0.240 2 48962782 missense variant C/T snv 0.57 0.57 0.020 1.000 2 2009 2014
Oligospermia
CUI: C0028960
Disease: Oligospermia
72 0.708 0.240 2 48962782 missense variant C/T snv 0.57 0.57 0.020 1.000 2 2010 2011
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
757 0.708 0.240 2 48962782 missense variant C/T snv 0.57 0.57 0.020 1.000 2 2009 2014
Anovulatory (finding)
CUI: C0429468
Disease: Anovulatory (finding)
8 0.708 0.240 2 48962782 missense variant C/T snv 0.57 0.57 0.010 1.000 1 2014 2014
Azoospermia
CUI: C0004509
Disease: Azoospermia
70 0.708 0.240 2 48962782 missense variant C/T snv 0.57 0.57 0.010 1.000 1 2019 2019
Disorder of endocrine ovary
CUI: C0154208
Disease: Disorder of endocrine ovary
1 0.708 0.240 2 48962782 missense variant C/T snv 0.57 0.57 0.010 1.000 1 2006 2006
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
283 0.708 0.240 2 48962782 missense variant C/T snv 0.57 0.57 0.010 1 2008 2008
Malignant Testicular Germ Cell Tumor
62 0.708 0.240 2 48962782 missense variant C/T snv 0.57 0.57 0.010 1.000 1 2018 2018
Osteoporosis
CUI: C0029456
Disease: Osteoporosis
182 0.708 0.240 2 48962782 missense variant C/T snv 0.57 0.57 0.010 1.000 1 2010 2010
Osteoporosis, Postmenopausal
CUI: C0029458
Disease: Osteoporosis, Postmenopausal
38 0.708 0.240 2 48962782 missense variant C/T snv 0.57 0.57 0.010 1.000 1 2010 2010