Extended Data Fig. 2: Regional association plots of the significant variants in X. | Nature Neuroscience

Extended Data Fig. 2: Regional association plots of the significant variants in X.

From: An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank

Extended Data Fig. 2

First row: Region around rs2272737 (P = 3.5 × 10−21). This variant is an eQTL of FAM58A. Second row: Region around rs62595479 (P = 8.2 × 10−17). This variant is located in a pseudoautosomal region (PAR1) of X, in an intron of DHRSX. Third row: Region around rs644138 (P = 4.8 × 10−15). This variant is in an intron of SPRY3 (and is an eQTL in brain tissue of various genes). Bottom row: Region around rs12843772 (P = 5.1 × 10−12) located ≤150 bp from ZIC3. The genomic positions of the loci and genes are based on Human Genome build hg19. Regions considered include all loci within 10 kbp of the hit.

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