V rs827382 | |||
Location: 10:8677306 Cytogenetic region:10p14 Most severe consequence: Intergenic variant Mapped gene(s): RNA5SP299,LINC02676 Associations 1 Studies 1 |
G RNA5SP299 | |||
Description: RNA, 5S ribosomal pseudogene 299 Associations 96 Studies 86 |
G LINC02676 | |||
Description: long intergenic non-protein coding RNA 2676 Associations 331 Studies 219 |