G WRAP53 | |||
Description: WD repeat containing antisense to TP53 Associations 15 Studies 12 |
V rs7640 | |||
Location: 17:7703404 Cytogenetic region:17p13.1 Most severe consequence: Missense variant Mapped gene(s): WRAP53 Associations 2 Studies 2 |
V rs34289079 | |||
Location: 17:7690001 Cytogenetic region:17p13.1 Most severe consequence: Intron variant Mapped gene(s): WRAP53 Associations 2 Studies 2 |
V rs12939910 | |||
Location: 17:7695942 Cytogenetic region:17p13.1 Most severe consequence: Intron variant Mapped gene(s): WRAP53 Associations 3 Studies 3 |
V rs9914473 | |||
Location: 17:7695548 Cytogenetic region:17p13.1 Most severe consequence: Intron variant Mapped gene(s): WRAP53 Associations 2 Studies 2 |
V rs183294622 | |||
Location: 17:7700066 Cytogenetic region:17p13.1 Most severe consequence: Intron variant Mapped gene(s): WRAP53 Associations 1 Studies 1 |
V rs2287497 | |||
Location: 17:7689462 Cytogenetic region:17p13.1 Most severe consequence: Intron variant Mapped gene(s): WRAP53 Associations 1 Studies 1 |
V rs200805760 | |||
Location: 17:7689680 Cytogenetic region:17p13.1 Most severe consequence: Synonymous variant Mapped gene(s): WRAP53 Associations 1 Studies 1 |
V rs17885803 | |||
Location: 17:7689164 Cytogenetic region:17p13.1 Most severe consequence: Intron variant Mapped gene(s): WRAP53 Associations 1 Studies 1 |
V rs12941981 | |||
Location: 17:7705144 Cytogenetic region:17p13.1 Most severe consequence: Regulatory region variant Mapped gene(s): WRAP53,EFNB3 Associations 1 Studies 1 |
V rs181067279 | |||
Location: 17:7687056 Cytogenetic region:17p13.1 Most severe consequence: 5 prime utr variant Mapped gene(s): WRAP53,TP53 Associations 1 Studies 1 |