V rs13202860 | |||
Location: 6:86445536 Cytogenetic region:6q14.3 Most severe consequence: Intergenic variant Mapped gene(s): HTR1E,RN7SL643P Associations 1 Studies 1 |
G RN7SL643P | |||
Description: RNA, 7SL, cytoplasmic 643, pseudogene Associations 43 Studies 37 |
G HTR1E | |||
Description: 5-hydroxytryptamine receptor 1E Associations 43 Studies 36 |