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