Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121909658
rs121909658
FSHR
0.050 GeneticVariation BEFREE A homozygous missense mutation, C566T, in the follicle stimulation hormone receptor (FSHR) gene has been linked to premature ovarian failure. 20086006

2010
dbSNP: rs121909658
rs121909658
FSHR
0.050 GeneticVariation BEFREE Toward gene therapy of primary ovarian failure: adenovirus expressing human FSH receptor corrects the Finnish C566T mutation. 18084009

2008
dbSNP: rs121909658
rs121909658
FSHR
0.050 GeneticVariation BEFREE An inactivating point mutation (Ala189Val) in the FSH receptor (FSHR) causes primary ovarian failure. 11756374

2002
dbSNP: rs121909658
rs121909658
FSHR
0.050 GeneticVariation BEFREE Neither of the two FSHR mutations (566C-->T or1255G-->A) was identified in 40 other Finnish patients with premature ovarian failure. 11889179

2002
dbSNP: rs121909658
rs121909658
FSHR
0.050 GeneticVariation BEFREE No evidence of the inactivating mutation (C566T) in the follicle-stimulating hormone receptor gene in Brazilian women with premature ovarian failure. 9757892

1998