List of variants in gene MDM4 reported as uncertain significance 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_002393.5(MDM4):c.1045A>G (p.Ile349Val)	rs1346731264	0.00001
NM_002393.5(MDM4):c.1147T>C (p.Ser383Pro)	rs2102456822

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