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. 2016 May 12;12(5):e1006000. doi: 10.1371/journal.pgen.1006000

Fig 3. Fine-mapping of candidate SNVs shows the strongest association within the CAMKK2 gene.

Fig 3

Genotyping of 56 candidate SNVs showed the strongest association within an intron of CAMKK2 for three tests: Including all glioma cases and controls (A), excluding all fixed breed samples (B), and assigning all fixed breed samples a status as cases (C). Second strongest association was seen in an intron of DENR, and in the gene P2RX7 where one SNV was non-synonymous coding.