List of variants in gene TP53 reported as uncertain significance by National Health Laboratory Service, Universitas Academic Hospital and University of the Free State

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.116C>T (p.Ala39Val)	rs1353016807
NM_000546.6(TP53):c.782+89del	rs2073229980
NM_000546.6(TP53):c.97-52G>A	rs540683791

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