G JPH3 | |||
Description: junctophilin 3 Associations 55 Studies 54 |
V rs34975147 | |||
Location: 16:87644970 Cytogenetic region:16q24.2 Most severe consequence: Synonymous variant Mapped gene(s): JPH3 Associations 1 Studies 1 |
V rs67163887 | |||
Location: 16:87660435 Cytogenetic region:16q24.2 Most severe consequence: Intron variant Mapped gene(s): JPH3 Associations 1 Studies 1 |
V rs117760708 | |||
Location: 16:87653662 Cytogenetic region:16q24.2 Most severe consequence: Intron variant Mapped gene(s): JPH3 Associations 1 Studies 1 |
V rs864839 | |||
Location: 16:87637813 Cytogenetic region:16q24.2 Most severe consequence: Intron variant Mapped gene(s): JPH3 Associations 2 Studies 2 |
V rs8051448 | |||
Location: 16:87644835 Cytogenetic region:16q24.2 Most severe consequence: Synonymous variant Mapped gene(s): JPH3 Associations 1 Studies 1 |
V rs200680880 | |||
Location: 16:87657558 Cytogenetic region:16q24.2 Most severe consequence: Intron variant Mapped gene(s): JPH3 Associations 1 Studies 1 |
V rs79613350 | |||
Location: 16:87640825 Cytogenetic region:16q24.2 Most severe consequence: Intron variant Mapped gene(s): JPH3 Associations 1 Studies 1 |
V rs117037877 | |||
Location: 16:87691035 Cytogenetic region:16q24.2 Most severe consequence: Intron variant Mapped gene(s): JPH3 Associations 1 Studies 1 |
V rs146846403 | |||
Location: 16:87609135 Cytogenetic region:16q24.2 Most severe consequence: Intron variant Mapped gene(s): JPH3 Associations 1 Studies 1 |
V rs7206657 | |||
Location: 16:87634866 Cytogenetic region:16q24.2 Most severe consequence: Intron variant Mapped gene(s): JPH3 Associations 1 Studies 1 |
V rs145661344 | |||
Location: 16:87679994 Cytogenetic region:16q24.2 Most severe consequence: Intron variant Mapped gene(s): JPH3 Associations 1 Studies 1 |
V rs144930872 | |||
Location: 16:87661926 Cytogenetic region:16q24.2 Most severe consequence: Intron variant Mapped gene(s): JPH3 Associations 1 Studies 1 |
V rs76960347 | |||
Location: 16:87644157 Cytogenetic region:16q24.2 Most severe consequence: Intron variant Mapped gene(s): JPH3 Associations 2 Studies 2 |
V rs56376716 | |||
Location: 16:87665947 Cytogenetic region:16q24.2 Most severe consequence: Intron variant Mapped gene(s): JPH3 Associations 1 Studies 1 |
V rs9924812 | |||
Location: 16:87660553 Cytogenetic region:16q24.2 Most severe consequence: Intron variant Mapped gene(s): JPH3 Associations 1 Studies 1 |
V rs12445022 | |||
Location: 16:87541726 Cytogenetic region:16q24.2 Most severe consequence: Regulatory region variant Mapped gene(s): ZCCHC14-DT,JPH3 Associations 24 Studies 24 |
V rs8052831 | |||
Location: 16:87544433 Cytogenetic region:16q24.2 Most severe consequence: Intergenic variant Mapped gene(s): ZCCHC14-DT,JPH3 Associations 3 Studies 3 |
V rs4081947 | |||
Location: 16:87546264 Cytogenetic region:16q24.2 Most severe consequence: Intergenic variant Mapped gene(s): ZCCHC14-DT,JPH3 Associations 2 Studies 2 |
V rs73251207 | |||
Location: 16:87582215 Cytogenetic region:16q24.2 Most severe consequence: Regulatory region variant Mapped gene(s): ZCCHC14-DT,JPH3 Associations 1 Studies 1 |
V rs862225 | |||
Location: 16:87571155 Cytogenetic region:16q24.2 Most severe consequence: Regulatory region variant Mapped gene(s): ZCCHC14-DT,JPH3 Associations 1 Studies 1 |
V rs149149942 | |||
Location: 16:87568645 Cytogenetic region:16q24.2 Most severe consequence: Intergenic variant Mapped gene(s): ZCCHC14-DT,JPH3 Associations 1 Studies 1 |
V rs8053397 | |||
Location: 16:87539862 Cytogenetic region:16q24.2 Most severe consequence: Intergenic variant Mapped gene(s): ZCCHC14-DT,JPH3 Associations 2 Studies 2 |
V rs13335533 | |||
Location: 16:87531358 Cytogenetic region:16q24.2 Most severe consequence: Intergenic variant Mapped gene(s): ZCCHC14-DT,JPH3 Associations 1 Studies 1 |
V rs11645728 | |||
Location: 16:87522482 Cytogenetic region:16q24.2 Most severe consequence: Intergenic variant Mapped gene(s): ZCCHC14-DT,JPH3 Associations 3 Studies 3 |
T blood protein measurement EFO_0007937 | |||
quantification of the levels of some protein in a blood sample Associations 20444 Studies 8346 |