G MYL3 | |||
Description: myosin light chain 3 Associations 21 Studies 20 |
V rs1077216 | |||
Location: 3:46850671 Cytogenetic region:3p21.31 Most severe consequence: Intergenic variant Mapped gene(s): MYL3 Associations 1 Studies 1 |
V rs76770574 | |||
Location: 3:46866428 Cytogenetic region:3p21.31 Most severe consequence: 5 prime utr variant Mapped gene(s): MYL3 Associations 1 Studies 1 |
V rs144261207 | |||
Location: 3:46869103 Cytogenetic region:3p21.31 Most severe consequence: Intron variant Mapped gene(s): MYL3 Associations 1 Studies 1 |
V rs56387622 | |||
Location: 3:46846708 Cytogenetic region:3p21.31 Most severe consequence: Regulatory region variant Mapped gene(s): MYL3 Associations 1 Studies 1 |
V rs6768627 | |||
Location: 3:46853886 Cytogenetic region:3p21.31 Most severe consequence: Intergenic variant Mapped gene(s): MYL3 Associations 2 Studies 2 |
V rs6772151 | |||
Location: 3:46855009 Cytogenetic region:3p21.31 Most severe consequence: Intergenic variant Mapped gene(s): MYL3 Associations 3 Studies 3 |
V rs73065147 | |||
Location: 3:46853449 Cytogenetic region:3p21.31 Most severe consequence: Intergenic variant Mapped gene(s): MYL3 Associations 3 Studies 3 |
V rs78595810 | |||
Location: 3:46868322 Cytogenetic region:3p21.31 Most severe consequence: Intron variant Mapped gene(s): MYL3 Associations 2 Studies 2 |
V rs111289888 | |||
Location: 3:46855965 Cytogenetic region:3p21.31 Most severe consequence: Intergenic variant Mapped gene(s): MYL3 Associations 2 Studies 2 |
V rs67529903 | |||
Location: 3:46846981 Cytogenetic region:3p21.31 Most severe consequence: Regulatory region variant Mapped gene(s): MYL3 Associations 1 Studies 1 |
V rs3792557 | |||
Location: 3:46861553 Cytogenetic region:3p21.31 Most severe consequence: Intron variant Mapped gene(s): MYL3 Associations 1 Studies 1 |
V rs74779174 | |||
Location: 3:46874010 Cytogenetic region:3p21.31 Most severe consequence: Intron variant Mapped gene(s): MYL3 Associations 1 Studies 1 |
V rs78629618 | |||
Location: 3:46838640 Cytogenetic region:3p21.31 Most severe consequence: Intergenic variant Mapped gene(s): PRSS42P,MYL3 Associations 2 Studies 2 |
T level of myosin light chain 3 in blood serum OBA_2040425 | |||
The amount of a myosin light chain 3 when measured in blood serum. Associations 27 Studies 3 |