FST, follistatin, 10468

N. diseases: 182; N. variants: 7
Disease: Polycystic Ovary Syndrome ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1062809
rs1062809 		1.000 0.120 5 53484261 missense variant C/A;G snv
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2007 2007
dbSNP: rs1127760
rs1127760 		1.000 0.120 5 53484287 missense variant T/A snv
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2007 2007
dbSNP: rs1127761
rs1127761 		1.000 0.120 5 53484289 stop gained T/A;C snv 2.8E-05
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2007 2007
dbSNP: rs11745088
rs11745088 		1.000 0.120 5 53483680 missense variant G/C snv 4.4E-03 4.2E-03
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2007 2007
dbSNP: rs1423560
rs1423560 		1.000 0.120 5 53479932 upstream gene variant G/A;T snv
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2007 2007
dbSNP: rs3797297
rs3797297 		1.000 0.120 5 53481826 intron variant G/T snv 0.18
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2007 2007