SYVN1
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
1164900270rs3825073GTrs38250739.43E-05Non-alcoholic fatty liver disease histology (other)HPOID:0001397|HPOID:0006561DOID:9452CintronGWASdb_trait
1164900270rs3825073GTrs38250732.80E-05Urinary metabolitesHPOID:0000079DOID:557CintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000162298.17 SYVN1 608046