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Fig. 3 | Genetics Selection Evolution

Fig. 3

From: Confirmation of a non-synonymous SNP in PNPLA8 as a candidate causal mutation for Weaver syndrome in Brown Swiss cattle

Fig. 3

Familial relationships, genotypes and haplotype structure of animal W0277 and its progeny. Haplotypes in red represent the common Weaver haplotype identified by homozygosity mapping (48,688,283–50,412,884 bp), haplotypes in green represent the haplotype that was passed down from animal W0380 to W0277 and inherited by its progeny and haplotypes in grey represent all haplotypes that were inherited from non-carrier and non-affected ancestors. Letters in rectangles represent the animals’ genotypes for the SNP at position 49,878,773 bp (rs800397662) with C as the reference allele and T as the alternative allele

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