Fig. 1 | European Journal of Human Genetics

Fig. 1

From: Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locus

Fig. 1

Regional conditional association plot of the new genome-wide significant HSCR variant. a Association results at RET locus before the conditional analysis. b Association results when conditioning on the RET lead SNP (rs2505994). Color-coded linkage disequilibrium is shown for the top conditional associated SNP rs144432435—in purple). The x-axis represents the chromosome 10 region (hg19 assembly) surrounding the new hit, while the y-axis represents the strength of the association in −log10 (P value) (see color fig online)

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