G SPRED1 | |||
Description: sprouty related EVH1 domain containing 1 Associations 20 Studies 18 |
V rs7175472 | |||
Location: 15:38254781 Cytogenetic region:15q14 Most severe consequence: Intron variant Mapped gene(s): SPRED1 Associations 1 Studies 1 |
V rs3938236 | |||
Location: 15:38253524 Cytogenetic region:15q14 Most severe consequence: Intron variant Mapped gene(s): SPRED1 Associations 1 Studies 1 |
V rs11853312 | |||
Location: 15:38334274 Cytogenetic region:15q14 Most severe consequence: Intron variant Mapped gene(s): SPRED1 Associations 1 Studies 1 |
V rs79896452 | |||
Location: 15:38297453 Cytogenetic region:15q14 Most severe consequence: Intron variant Mapped gene(s): SPRED1 Associations 1 Studies 1 |
V rs2056501 | |||
Location: 15:38284033 Cytogenetic region:15q14 Most severe consequence: Intron variant Mapped gene(s): SPRED1 Associations 1 Studies 1 |
V rs4457952 | |||
Location: 15:38280861 Cytogenetic region:15q14 Most severe consequence: Intron variant Mapped gene(s): SPRED1 Associations 1 Studies 1 |
V rs940026 | |||
Location: 15:38253598 Cytogenetic region:15q14 Most severe consequence: Intron variant Mapped gene(s): SPRED1 Associations 1 Studies 1 |
V rs148021236 | |||
Location: 15:38277456 Cytogenetic region:15q14 Most severe consequence: Intron variant Mapped gene(s): SPRED1 Associations 1 Studies 1 |
V rs2056507 | |||
Location: 15:38274242 Cytogenetic region:15q14 Most severe consequence: Intron variant Mapped gene(s): SPRED1 Associations 1 Studies 1 |
V rs8029989 | |||
Location: 15:38441646 Cytogenetic region:15q14 Most severe consequence: Intergenic variant Mapped gene(s): SPRED1,FAM98B Associations 1 Studies 1 |
V rs6495962 | |||
Location: 15:38359831 Cytogenetic region:15q14 Most severe consequence: Intergenic variant Mapped gene(s): SPRED1,FAM98B Associations 2 Studies 2 |
V rs1542900 | |||
Location: 15:38236971 Cytogenetic region:15q14 Most severe consequence: Intergenic variant Mapped gene(s): SPRED1,LINC02895 Associations 2 Studies 2 |
V rs11635385 | |||
Location: 15:38370003 Cytogenetic region:15q14 Most severe consequence: Intergenic variant Mapped gene(s): SPRED1,FAM98B Associations 1 Studies 1 |
V rs75844534 | |||
Location: 15:38374916 Cytogenetic region:15q14 Most severe consequence: Intergenic variant Mapped gene(s): SPRED1,FAM98B Associations 1 Studies 1 |
V rs74843685 | |||
Location: 15:38392676 Cytogenetic region:15q14 Most severe consequence: Intergenic variant Mapped gene(s): SPRED1,FAM98B Associations 1 Studies 1 |
V rs4923780 | |||
Location: 15:38251762 Cytogenetic region:15q14 Most severe consequence: Intergenic variant Mapped gene(s): SPRED1,LINC02895 Associations 1 Studies 1 |
V rs4924248 | |||
Location: 15:38364053 Cytogenetic region:15q14 Most severe consequence: Intergenic variant Mapped gene(s): SPRED1,FAM98B Associations 1 Studies 1 |
V rs12148176 | |||
Location: 15:38363879 Cytogenetic region:15q14 Most severe consequence: Intergenic variant Mapped gene(s): SPRED1,FAM98B Associations 1 Studies 1 |
T blood protein measurement EFO_0007937 | |||
quantification of the levels of some protein in a blood sample Associations 20444 Studies 8346 |