LASP1
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
1737037718rs11653086GTrs116530867.80E-06Urinary metabolitesHPOID:0000079DOID:557TintronGWASdb_trait
1737042006rs3785461GArs37854612.56E-04Hearing functionHPOID:0000365DOID:2742GintronGWASdb_trait
1737062847rs11659022AGrs116590226.27E-04Multiple complex diseasesHPOID:0000118NAAintronGWASdb_trait
1737064348rs82977GArs829778.39E-04Amyotrophic Lateral SclerosisHPOID:0007354DOID:332AintronGWASdb_trait
1737064348rs82977GArs829771.19E-05Alcohol and nictotine co-dependenceHPOID:0000707DOID:0050741|DOID:0050742AintronGWASdb_trait
1737075506rs660413GArs6604133.82E-04Suicide attempts in bipolar disorderHPOID:0007302DOID:3312CUTR-3GWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000002834.17 LASP1 602920