G TMC6 | |||
Description: transmembrane channel like 6 Associations 130 Studies 113 |
P Genome-wide meta-analysis in Japanese populations identifies novel variants at the TMC6-TMC8 and SIX3-SIX2 loci associated with HbA1c. | |||
Hachiya T et al. 2017 Sci Rep PMID:29170429 Associations 7 Studies 1 |
V rs2613514 | |||
Location: 17:78114437 Cytogenetic region:17q25.3 Most severe consequence: Intron variant Mapped gene(s): TMC6 Associations 1 Studies 1 |
V rs2748425 | |||
Location: 17:78128765 Cytogenetic region:17q25.3 Most severe consequence: Intron variant Mapped gene(s): TMC6 Associations 16 Studies 16 |
V rs3794738 | |||
Location: 17:78123212 Cytogenetic region:17q25.3 Most severe consequence: Intron variant Mapped gene(s): TMC6 Associations 5 Studies 5 |
V rs2748424 | |||
Location: 17:78128784 Cytogenetic region:17q25.3 Most severe consequence: Intron variant Mapped gene(s): TMC6 Associations 16 Studies 16 |
V rs2253277 | |||
Location: 17:78112992 Cytogenetic region:17q25.3 Most severe consequence: 3 prime utr variant Mapped gene(s): TMC6 Associations 1 Studies 1 |
V rs761772 | |||
Location: 17:78125997 Cytogenetic region:17q25.3 Most severe consequence: Intron variant Mapped gene(s): TMC6 Associations 1 Studies 1 |
V rs453922 | |||
Location: 17:78130526 Cytogenetic region:17q25.3 Most severe consequence: Intron variant Mapped gene(s): TMC6 Associations 1 Studies 1 |
V rs2748427 | |||
Location: 17:78125783 Cytogenetic region:17q25.3 Most severe consequence: Missense variant Mapped gene(s): TMC6 Associations 20 Studies 20 |
V rs429216 | |||
Location: 17:78130123 Cytogenetic region:17q25.3 Most severe consequence: Intron variant Mapped gene(s): TMC6 Associations 7 Studies 7 |
V rs2613522 | |||
Location: 17:78123984 Cytogenetic region:17q25.3 Most severe consequence: Splice donor 5th base variant Mapped gene(s): TMC6 Associations 7 Studies 7 |
V rs3834968 | |||
Location: 17:78128730 Cytogenetic region:17q25.3 Most severe consequence: 5 prime utr variant Mapped gene(s): TMC6 Associations 8 Studies 8 |
V rs1474865 | |||
Location: 17:78122806 Cytogenetic region:17q25.3 Most severe consequence: Intron variant Mapped gene(s): TMC6 Associations 7 Studies 7 |
V rs12449858 | |||
Location: 17:78125237 Cytogenetic region:17q25.3 Most severe consequence: Missense variant Mapped gene(s): TMC6 Associations 7 Studies 7 |
V rs454139 | |||
Location: 17:78130013 Cytogenetic region:17q25.3 Most severe consequence: Intron variant Mapped gene(s): TMC6 Associations 2 Studies 2 |
V rs3813026 | |||
Location: 17:78127447 Cytogenetic region:17q25.3 Most severe consequence: Intron variant Mapped gene(s): TMC6 Associations 1 Studies 1 |
V rs3841687 | |||
Location: 17:78119398 Cytogenetic region:17q25.3 Most severe consequence: Splice region variant Mapped gene(s): TMC6 Associations 1 Studies 1 |
V rs2613518 | |||
Location: 17:78118773 Cytogenetic region:17q25.3 Most severe consequence: Intron variant Mapped gene(s): TMC6 Associations 1 Studies 1 |
V rs200350733 | |||
Location: 17:78129114 Cytogenetic region:17q25.3 Most severe consequence: Intron variant Mapped gene(s): TMC6 Associations 1 Studies 1 |
V rs379149 | |||
Location: 17:78130505 Cytogenetic region:17q25.3 Most severe consequence: Intron variant Mapped gene(s): TMC6 Associations 4 Studies 4 |
V rs383603 | |||
Location: 17:78131350 Cytogenetic region:17q25.3 Most severe consequence: 5 prime utr variant Mapped gene(s): TMC6,TMC8 Associations 9 Studies 8 |
V rs3834968 (rs558567978) | |||
Location: 17:78128730 Cytogenetic region:17q25.3 Most severe consequence: 5 prime utr variant Mapped gene(s): TMC6 Associations 14 Studies 14 |