V rs429358 | |||
Location: 19:44908684 Cytogenetic region:19q13.32 Most severe consequence: Missense variant Mapped gene(s): APOE Associations 1000 Studies 983 |
G APOE | |||
Description: apolipoprotein E Associations 3038 Studies 2395 |
T APOE carrier status EFO_0007659 | |||
quantification of the presence or absence of apolipoprotein E (APOE) in an individual Associations 136 Studies 9 |