G CIB2 | |||
Description: calcium and integrin binding family member 2 Associations 2 Studies 2 |
V rs8040395 | |||
Location: 15:78131137 Cytogenetic region:15q25.1 Most severe consequence: Intron variant Mapped gene(s): CIB2 Associations 1 Studies 1 |
V rs141932061 | |||
Location: 15:78105833 Cytogenetic region:15q25.1 Most severe consequence: Missense variant Mapped gene(s): CIB2 Associations 1 Studies 1 |