NSMAF
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
859508580rs11994937CTrs119949375.00E-06IMMUNOGLOBULIN GGLYCOSYLTRANSFERASESIgG glycosylationHPOID:0010701DOID:2531|DOID:417TintronGWASdb_drug
859508580rs11994937CTrs119949375.00E-06IgG glycosylationHPOID:0010701DOID:2531|DOID:417TintronGWASdb_trait
859571287rs973807CTrs9738071.49E-04Amyotrophic Lateral SclerosisHPOID:0007354DOID:332TintronGWASdb_trait
859571287rs973807CTrs9738071.49E-05Serum metabolitesHPOID:0011111NATintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000035681.7 NSMAF 603043