. . . . . . . . . . . . "[A low-frequency (1.47%) variant in intron 1 of CCND2, rs76895963[G], reduces risk of T2D by half (odds ratio (OR) = 0.53, P = 5.0 A 10(-21)) and is correlated with increased CCND2 expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2015-02-21"^^ . . "Gene-disease associations manually curated."@en . "DisGeNET evidence - CURATED"@en . "2015-08-25T14:37:46+02:00"^^ . . . . . . . . . . . "v3.0.0.0" . "v3.0.0" .