rs1376873864, BRD2

N. diseases: 2
Disease: Premature Menopause ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Premature Menopause
CUI: C0025322
Disease: Premature Menopause
0.030 GeneticVariation BEFREE Although the reduction of inhibin B bioactivity by the INHA G769A mutation is clearly not the only cause, evidence suggests that this change may serve as a susceptibility factor, increasing the likelihood of POF. 19752047 2010
Premature Menopause
CUI: C0025322
Disease: Premature Menopause
0.030 GeneticVariation BEFREE This study supports the hypothesis that the INHA 769G>A variant may increase susceptibility to POF with impaired inhibin B bioactivity and provides insight into the complex aetiology of POF. 17933751 2007
Premature Menopause
CUI: C0025322
Disease: Premature Menopause
0.030 GeneticVariation BEFREE Our results indicate that -16C>T and 769G>A variants in INHalpha gene may not be associated to POF disease. 16396934 2006