Barely Significant
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Association of prolactin receptor (PRLR) variants with prolactinomas.

Hum Mol Genet · 2019 · PMC6400049 · PMID 30445560

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highly significantno p-value reported
5 ) but is in complete LD with the gain-of-function Asn492Ile mutant PRLR, is also likely to be a benign polymorphism, despite its highly significant association with prolactinomas ( Table 1 ).

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