[A variant at 9p21 near CDKN2A and CDKN2B also confers susceptibility to BCC (rs2151280C; OR = 1.19, P = 6.9 x 10(-9)), as does rs157935T at 7q32 near the imprinted gene KLF14 (OR = 1.23, P = 5.7 x 10(-10)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
Gene-disease associations inferred from text-mining the literature.
DisGeNET evidence - LITERATURE