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Anti-Müllerian hormone (AMH) is an essential messenger of sexual differentiation in the foetus and is an emerging biomarker of postnatal reproductive function in females. Due to a paucity of adequately sized studies, the genetic determinants of circulating AMH levels are poorly characterized. In samples from 2815 adolescents aged 15 from the ALSPAC study, we performed the first genome-wide association study of serum AMH levels across a set of ∼9  m  ‘1000 Genomes Reference Panel’ imputed genetic variants. Genetic variants at the  AMH  protein-coding gene showed considerable allelic heterogeneity, with both common variants [rs4807216 ( P  Male  = 2 × 10 −49 , Beta: ∼0.9 SDs per allele), rs8112524 ( P  Male  = 3 × 10 −8 , Beta: ∼0.25)] and low-frequency variants [rs2385821 ( P  Male  = 6 × 10 −31 , Beta: ∼1.2, frequency 3.6%)] independently associated with apparently large effect sizes in males, but not females. For all three SNPs, we highlight mechanistic links to  AMH  gene function and demonstrate highly significant sex interactions ( P  Het  0.0003–6.3 × 10 −12 ), culminating in contrasting estimates of trait variance explained (24.5% in males versus 0.8% in females). Using these SNPs as a genetic proxy for AMH levels, we found no evidence in additional datasets to support a biological role for AMH in complex traits and diseases in men.

Genome-wide association study identifies common and low-frequency variants at the AMH gene locus that strongly predict serum AMH levels in males