Extended Data Fig. 7: Shared haplotype for RAB32 p.S71R. | Nature Genetics

Extended Data Fig. 7: Shared haplotype for RAB32 p.S71R.

From: Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson’s disease

Extended Data Fig. 7

The figure shows the shared haplotype in a ± 250-kb window surrounding the p.S71R variant based on common markers on the Infinium Global Diversity Array-8 (available for 16 out of 18 p.S71R carriers). The y-axis shows SNP IDs with the distance to the p.S71R variant in parentheses, and the x-axis shows the p.S71R genotype (both alleles are shown for the homozygous carrier). The minimal common region extends from -131,546 bp downstream to 182,121 bp upstream of the p.S71R variant.

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