rs11668344, TMEM150B

N. diseases: 4
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.
Age at menopause
CUI: C1629609
Disease: Age at menopause
209 0.925 0.120 19 55322296 intron variant A/G snv 0.35 0.800 1.000 3 2012 2015
Age at menarche
CUI: C1314691
Disease: Age at menarche
591 0.925 0.120 19 55322296 intron variant A/G snv 0.35 0.700 1.000 1 2018 2018
Ovarian Failure, Premature
CUI: C0085215
Disease: Ovarian Failure, Premature
115 0.925 0.120 19 55322296 intron variant A/G snv 0.35 0.010 1.000 1 2019 2019
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
363 0.925 0.120 19 55322296 intron variant A/G snv 0.35 0.010 1 2015 2015