List of variants reported as uncertain significance for acute megakaryoblastic leukemia

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-ND6):m.14372C>A	rs1556424431
NM_001099.5(ACP3):c.849CAT[1] (p.Ile284del)	rs864309497
NM_001346413.3(PCF11):c.3618del (p.Phe1206fs)	rs864309498
NM_003048.6(SLC9A2):c.2173del (p.Gln725fs)	rs864309496
NM_022904.3(RASAL3):c.-5C>G	rs76267899
NM_024535.5(CORO7):c.2772+50C>T	rs1555468179
NM_153487.4(MDGA1):c.2674T>G (p.Phe892Val)	rs864309493

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.