List of variants in gene MECOM reported as likely pathogenic for hematologic disorder

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

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_004991.4(MECOM):c.1678C>T (p.Gln560Ter)	rs1577005203
NM_004991.4(MECOM):c.2398A>T (p.Lys800Ter)	rs1475580175
NM_004991.4(MECOM):c.2772-4A>G
NM_004991.4(MECOM):c.739C>T (p.Gln247Ter)

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