List of variants in gene combination ACBD5, MASTL reported as uncertain significance for hematologic disorder

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

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001172303.3(MASTL):c.2521G>A (p.Glu841Lys)	rs1188516311	0.00001
NM_001172303.3(MASTL):c.2526T>C (p.Asn842=)	rs886046961	0.00001
NM_001172303.3(MASTL):c.*203T>A	rs886046962
NM_001172303.3(MASTL):c.*252T>C	rs886046963
NM_001172303.3(MASTL):c.2517C>T (p.Asp839=)	rs886046960

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