G TNNC1 | |||
Description: troponin C1, slow skeletal and cardiac type Associations 2 Studies 2 |
V rs115716895 | |||
Location: 3:52452886 Cytogenetic region:3p21.1 Most severe consequence: Intron variant Mapped gene(s): TNNC1 Associations 1 Studies 1 |
V rs3821838 | |||
Location: 3:52455033 Cytogenetic region:3p21.1 Most severe consequence: Regulatory region variant Mapped gene(s): TNNC1,NISCH Associations 1 Studies 1 |