V rs9807334 | |||
Location: 18:50997791 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): SMAD4,ELAC1 Associations 2 Studies 2 |
G ELAC1 | |||
Description: elaC ribonuclease Z 1 Associations 8 Studies 8 |
G SMAD4 | |||
Description: SMAD family member 4 Associations 24 Studies 24 |