V rs7944004 | |||
Location: 11:2289922 Cytogenetic region:11p15.5 Most severe consequence: Intergenic variant Mapped gene(s): C11orf21,ASCL2 Associations 1 Studies 1 |
G C11orf21 | |||
Description: chromosome 11 open reading frame 21 Associations 62 Studies 61 |
G ASCL2 | |||
Description: achaete-scute family bHLH transcription factor 2 Associations 141 Studies 108 |