V rs9369898 | |||
Location: 6:49414480 Cytogenetic region:6p12.3 Most severe consequence: Intergenic variant Mapped gene(s): MMUT,EEF1A1P42 Associations 1 Studies 1 |
G MMUT | |||
Description: methylmalonyl-CoA mutase Associations 12 Studies 12 |
G EEF1A1P42 | |||
Description: eukaryotic translation elongation factor 1 alpha 1 pseudogene 42 Associations 7 Studies 7 |