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Fig. 1 | BMC Genomics

Fig. 1

From: Genome-wide association studies highlight novel risk loci for septal defects and left-sided congenital heart defects

Fig. 1

Lead SNPs associating with CHD identified in FinnGen R10. Manhattan plots of the different CHD categories: A general CHD, B septal defects, C left-sided lesions and D conotruncal defects, with genome-wide significant lead SNPs indicated, meaning the SNPs within a region with the highest association signal, as the other SNPs may only show association due to being in linkage disequilibrium (LD) with the lead signal

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BMC Genomics

ISSN: 1471-2164

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