Location: 15:54049268 Cytogenetic region:15q21.3 Most severe consequence: Intron variant Mapped gene(s): UNC13C
Associations 1 Studies 1
Description: unc-13 homolog CLocation: 15:53978201-54628707 Cytogenetic region: 15q21.3 Biotype: protein coding
Associations 90 Studies 70