<HashMap><database>EGA</database><scores/><additional><omics_type>Genomics</omics_type><study_type>Exome Sequencing</study_type><full_dataset_link>https://ega-archive.org/studies/EGAS00001005764</full_dataset_link><host>EGA</host><description>EGA study EGAS00001005764</description><dataset_title>Germline loss-of-function P2RY8 variants in SLE</dataset_title><repository>EGA</repository><category>restricted</category></additional><is_claimable>false</is_claimable><name>JEM 20211004R</name><description>Our mission is to undertake ground breaking research, combining fundamental science and strong clinical interactions, to uncover the mechanism of disease of our patients, ultimately to provide a diagnosis and improved treatments. SLE is an autoimmune disease with a strong genetic component. Genome-wide association studies (GWAS) have revealed that multiple common variants confer genetic susceptibility to SLE, defining key pathways involved in disease pathogenesis.</description><dates><updated>2021-11-16 13:33:21</updated></dates><accession>EGAS00001005764</accession><cross_references><TAXONOMY>9606</TAXONOMY><EGA>EGAD00001008330</EGA><EGA>EGAC00001002394</EGA></cross_references></HashMap>