G ATF6 | |||
Description: activating transcription factor 6 Associations 28 Studies 18 |
G ATF6-DT | |||
Description: ATF6 divergent transcript Associations 11 Studies 11 |
V rs3767633 | |||
Location: 1:161856825 Cytogenetic region:1q23.3 Most severe consequence: Intron variant Mapped gene(s): ATF6 Associations 1 Studies 1 |
V rs2340727 | |||
Location: 1:161976937 Cytogenetic region:1q23.3 Most severe consequence: Intergenic variant Mapped gene(s): ATF6 Associations 3 Studies 3 |
V rs10918270 | |||
Location: 1:161945711 Cytogenetic region:1q23.3 Most severe consequence: Intron variant Mapped gene(s): ATF6 Associations 1 Studies 1 |
V rs16849542 | |||
Location: 1:161816705 Cytogenetic region:1q23.3 Most severe consequence: Intron variant Mapped gene(s): ATF6 Associations 1 Studies 1 |
V rs3002626 | |||
Location: 1:161968102 Cytogenetic region:1q23.3 Most severe consequence: Intergenic variant Mapped gene(s): ATF6 Associations 1 Studies 1 |
V rs1962508 | |||
Location: 1:161975629 Cytogenetic region:1q23.3 Most severe consequence: Intergenic variant Mapped gene(s): ATF6 Associations 1 Studies 1 |
V rs114015046 | |||
Location: 1:161924490 Cytogenetic region:1q23.3 Most severe consequence: Intron variant Mapped gene(s): ATF6 Associations 1 Studies 1 |
V rs17450717 | |||
Location: 1:161929846 Cytogenetic region:1q23.3 Most severe consequence: Intron variant Mapped gene(s): ATF6 Associations 1 Studies 1 |
V rs116791819 | |||
Location: 1:161777251 Cytogenetic region:1q23.3 Most severe consequence: Intron variant Mapped gene(s): ATF6 Associations 2 Studies 2 |
V rs76652463 | |||
Location: 1:161772121 Cytogenetic region:1q23.3 Most severe consequence: Intron variant Mapped gene(s): ATF6 Associations 2 Studies 2 |
V rs115076617 | |||
Location: 1:161886152 Cytogenetic region:1q23.3 Most severe consequence: Intron variant Mapped gene(s): ATF6 Associations 2 Studies 2 |
V rs6695760 | |||
Location: 1:161915755 Cytogenetic region:1q23.3 Most severe consequence: Intron variant Mapped gene(s): ATF6 Associations 1 Studies 1 |
V rs28628087 | |||
Location: 1:161971681 Cytogenetic region:1q23.3 Most severe consequence: Intergenic variant Mapped gene(s): ATF6 Associations 4 Studies 4 |
V rs2490441 | |||
Location: 1:161965261 Cytogenetic region:1q23.3 Most severe consequence: Intergenic variant Mapped gene(s): ATF6 Associations 1 Studies 1 |
V rs77505094 | |||
Location: 1:161936103 Cytogenetic region:1q23.3 Most severe consequence: Intron variant Mapped gene(s): ATF6 Associations 1 Studies 1 |
V rs2490436 | |||
Location: 1:161967834 Cytogenetic region:1q23.3 Most severe consequence: Intergenic variant Mapped gene(s): ATF6 Associations 1 Studies 1 |
V rs953301 | |||
Location: 1:161749589 Cytogenetic region:1q23.3 Most severe consequence: Tf binding site variant Mapped gene(s): ATF6-DT Associations 1 Studies 1 |
V rs17452514 | |||
Location: 1:161981287 Cytogenetic region:1q23.3 Most severe consequence: Intergenic variant Mapped gene(s): OLFML2B,ATF6 Associations 2 Studies 2 |
V rs10918341 | |||
Location: 1:161980609 Cytogenetic region:1q23.3 Most severe consequence: Intergenic variant Mapped gene(s): OLFML2B,ATF6 Associations 1 Studies 1 |
V rs7529274 | |||
Location: 1:161978337 Cytogenetic region:1q23.3 Most severe consequence: Intergenic variant Mapped gene(s): OLFML2B,ATF6 Associations 1 Studies 1 |
V rs1340981 | |||
Location: 1:161741462 Cytogenetic region:1q23.3 Most severe consequence: Regulatory region variant Mapped gene(s): ATF6-DT,RN7SL466P Associations 1 Studies 1 |
V rs4657098 | |||
Location: 1:161744792 Cytogenetic region:1q23.3 Most severe consequence: Intergenic variant Mapped gene(s): ATF6-DT,RN7SL466P Associations 1 Studies 1 |
V rs7540096 | |||
Location: 1:161751561 Cytogenetic region:1q23.3 Most severe consequence: Intron variant Mapped gene(s): DUSP12,ATF6-DT Associations 1 Studies 1 |
V rs4657097 | |||
Location: 1:161744783 Cytogenetic region:1q23.3 Most severe consequence: Intergenic variant Mapped gene(s): ATF6-DT,RN7SL466P Associations 1 Studies 1 |
V rs10799941 | |||
Location: 1:161738404 Cytogenetic region:1q23.3 Most severe consequence: Intergenic variant Mapped gene(s): ATF6-DT,RN7SL466P Associations 1 Studies 1 |
V rs9787369 | |||
Location: 1:161739343 Cytogenetic region:1q23.3 Most severe consequence: Regulatory region variant Mapped gene(s): ATF6-DT,RN7SL466P Associations 4 Studies 4 |
V rs114499611 | |||
Location: 1:161745485 Cytogenetic region:1q23.3 Most severe consequence: Intergenic variant Mapped gene(s): ATF6-DT,RN7SL466P 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 |