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

Table 2 Comparison between clinical/genetic diagnosis and targeted genotyping for the SNP Chr4:50,858,538 bp

Animal ID	Clinical or genetic diagnosis from the 1990s	Genotype at
Animal ID	Clinical or genetic diagnosis from the 1990s	SNP_49878773	SNP_50858538
W0037	Carrier	CT	AA
W0246	Affected	TT	GA

Capital letters represent the animals’ genotypes (additional information on SNP_49878773 genotypes: C: reference allele, T: alternative allele; SNP_50858538 genotypes: G: reference allele, A: alternative allele)

ISSN: 1297-9686