G AARS1 | |||
Description: alanyl-tRNA synthetase 1 Associations 16 Studies 15 |
V rs12149660 | |||
Location: 16:70275334 Cytogenetic region:16q22.1 Most severe consequence: Intron variant Mapped gene(s): AARS1 Associations 7 Studies 7 |
V rs2070203 | |||
Location: 16:70269677 Cytogenetic region:16q22.1 Most severe consequence: Missense variant Mapped gene(s): AARS1 Associations 1 Studies 1 |
V rs775208 | |||
Location: 16:70282008 Cytogenetic region:16q22.1 Most severe consequence: Intron variant Mapped gene(s): AARS1 Associations 5 Studies 5 |
V rs34846578 | |||
Location: 16:70258896 Cytogenetic region:16q22.1 Most severe consequence: Intron variant Mapped gene(s): AARS1 Associations 1 Studies 1 |
V rs4985407 | |||
Location: 16:70251998 Cytogenetic region:16q22.1 Most severe consequence: 3 prime utr variant Mapped gene(s): AARS1 Associations 1 Studies 1 |
V rs35259849 (rs562771447) | |||
Location: 16:70274935 Cytogenetic region:16q22.1 Most severe consequence: Intron variant Mapped gene(s): AARS1 Associations 1 Studies 1 |
G METTL21C | |||
Description: methyltransferase 21C, AARS1 lysine Associations 12 Studies 7 |