G PLSCR3 | |||
Description: phospholipid scramblase 3 Associations 3 Studies 3 |
G TMEM256-PLSCR3 | |||
Description: TMEM256-PLSCR3 readthrough (NMD candidate) Associations 9 Studies 6 |
V rs3744549 | |||
Location: 17:7390396 Cytogenetic region:17p13.1 Most severe consequence: Missense variant Mapped gene(s): TMEM256-PLSCR3,PLSCR3 Associations 2 Studies 2 |
V rs570333094 | |||
Location: 17:7394650 Cytogenetic region:17p13.1 Most severe consequence: 3 prime utr variant Mapped gene(s): TMEM256-PLSCR3,PLSCR3 Associations 1 Studies 1 |
V rs150452493 | |||
Location: 17:7400489 Cytogenetic region:17p13.1 Most severe consequence: Intron variant Mapped gene(s): TMEM256-PLSCR3 Associations 2 Studies 1 |
V rs139552861 | |||
Location: 17:7404072 Cytogenetic region:17p13.1 Most severe consequence: Missense variant Mapped gene(s): TMEM256-PLSCR3,TMEM256 Associations 1 Studies 1 |
V rs71370494 | |||
Location: 17:7403755 Cytogenetic region:17p13.1 Most severe consequence: Intron variant Mapped gene(s): TMEM256-PLSCR3,TMEM256 Associations 1 Studies 1 |
V rs114576150 | |||
Location: 17:7404631 Cytogenetic region:17p13.1 Most severe consequence: Regulatory region variant Mapped gene(s): NLGN2,TMEM256-PLSCR3,TMEM256 Associations 2 Studies 2 |
T level of phospholipid scramblase 3 in blood serum OBA_2042933 | |||
The amount of a phospholipid scramblase 3 when measured in blood serum. Associations 4 Studies 3 |
T blood protein measurement EFO_0007937 | |||
quantification of the levels of some protein in a blood sample Associations 20444 Studies 8346 |