MYNN
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
3169492101rs10936599CTrs109365995.00E-07Celiac diseaseHPOID:0001438DOID:10608Ccds-synonGWASdb_trait
3169492101rs10936599CTrs109365993.00E-08Colorectal cancerHPOID:0100834DOID:9256Ccds-synonGWASdb_trait
3169492101rs10936599CTrs109365997.00E-07Multiple sclerosisHPOID:0000096|HPOID:0001967|HPOID:0009741|HPOID:0008664|HPOID:0001150|HPOID:0005450|HPOID:0005652|HPOID:0005686|HPOID:0005789|HPOID:0100923|HPOID:0100925|HPOID:0006623|HPOID:0100861|HPOID:0002694|HPOID:0004979|HPOID:0003881|HPOID:0003991|HPOID:0003854|HPOID:0003933|HPOID:0004030|HPOID:0100899|HPOID:0002634DOID:2377Ccds-synonGWASdb_trait
3169492101rs10936599CTrs109365993.00E-31Telomere lengthHPOID:0000118NACcds-synonGWASdb_trait
3169492101rs10936599CTrs109365991.52E-08Interstitial lung diseaseHPOID:0002088DOID:3082Ccds-synonGWASdb_trait
3169492101rs10936599CTrs109365993.90E-07Interstitial lung diseaseHPOID:0002088DOID:3082Ccds-synonGWASdb_trait
3169492101rs10936599CTrs109365999.00E-14Multiple myelomaHPOID:0006775DOID:9538Ccds-synonGWASdb_trait
3169492101rs10936599CTrs109365995.00E-09Bladder cancerHPOID:0002862DOID:4007Ccds-synonGWASdb_trait
3169492101rs10936599CTrs109365992.00E-09Chronic lymphocytic leukemiaHPOID:0005550DOID:1040Ccds-synonGWASdb_trait
3169497585rs1317082AGrs13170821.00E-08Telomere lengthHPOID:0000118NAAintronGWASdb_trait
3169497585rs1317082AGrs13170822.40E-08Interstitial lung diseaseHPOID:0002088DOID:3082AintronGWASdb_trait
3169497585rs1317082AGrs13170821.33E-19Telomere lengthHPOID:0000118NAAintronGWASdb_trait
3169497585rs1317082AGrs13170821.00E-09Multiple myelomaHPOID:0006775DOID:9538AintronGWASdb_trait
3169502180rs1920120TCrs19201203.11E-09Interstitial lung diseaseHPOID:0002088DOID:3082CintronGWASdb_trait
3169503432rs2141595CTrs21415951.86E-09Interstitial lung diseaseHPOID:0002088DOID:3082TintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000085274.15 MYNN 606042