G CEP152 | |||
Description: centrosomal protein 152 Associations 18 Studies 13 |
V rs16961557 | |||
Location: 15:48755931 Cytogenetic region:15q21.1 Most severe consequence: Missense variant Mapped gene(s): CEP152 Associations 1 Studies 1 |
V rs784411 | |||
Location: 15:48747600 Cytogenetic region:15q21.1 Most severe consequence: Intron variant Mapped gene(s): CEP152 Associations 1 Studies 1 |
V rs16961637 | |||
Location: 15:48781895 Cytogenetic region:15q21.1 Most severe consequence: Intron variant Mapped gene(s): CEP152 Associations 1 Studies 1 |
V rs16961587 | |||
Location: 15:48760612 Cytogenetic region:15q21.1 Most severe consequence: Intron variant Mapped gene(s): CEP152 Associations 1 Studies 1 |
V rs9302144 | |||
Location: 15:48767476 Cytogenetic region:15q21.1 Most severe consequence: Splice polypyrimidine tract variant Mapped gene(s): CEP152 Associations 2 Studies 2 |
V rs117143514 | |||
Location: 15:48807394 Cytogenetic region:15q21.1 Most severe consequence: Intron variant Mapped gene(s): CEP152 Associations 1 Studies 1 |
V rs17466389 | |||
Location: 15:48815443 Cytogenetic region:15q21.1 Most severe consequence: Intergenic variant Mapped gene(s): CEP152,SHC4 Associations 1 Studies 1 |
V rs2725544 | |||
Location: 15:48700700 Cytogenetic region:15q21.1 Most severe consequence: Intergenic variant Mapped gene(s): FBN1-DT,CEP152 Associations 1 Studies 1 |
V rs1848053 | |||
Location: 15:48655765 Cytogenetic region:15q21.1 Most severe consequence: Intergenic variant Mapped gene(s): FBN1-DT,CEP152 Associations 1 Studies 1 |
V rs7175415 | |||
Location: 15:48698392 Cytogenetic region:15q21.1 Most severe consequence: Intergenic variant Mapped gene(s): FBN1-DT,CEP152 Associations 1 Studies 1 |
V rs8042197 | |||
Location: 15:48656094 Cytogenetic region:15q21.1 Most severe consequence: Intergenic variant Mapped gene(s): FBN1-DT,CEP152 Associations 4 Studies 4 |
V rs784409 | |||
Location: 15:48704085 Cytogenetic region:15q21.1 Most severe consequence: Intergenic variant Mapped gene(s): FBN1-DT,CEP152 Associations 1 Studies 1 |
V rs12440930 | |||
Location: 15:48712853 Cytogenetic region:15q21.1 Most severe consequence: Intergenic variant Mapped gene(s): FBN1-DT,CEP152 Associations 1 Studies 1 |
V rs16961323 | |||
Location: 15:48666885 Cytogenetic region:15q21.1 Most severe consequence: Intergenic variant Mapped gene(s): FBN1-DT,CEP152 Associations 1 Studies 1 |
T level of centrosomal protein of 152 kDa in blood OBA_2051299 | |||
The amount of a centrosomal protein of 152 kDa when measured in blood. Associations 1 Studies 2 |