List of variants in gene TP53 reported as pathogenic for anemia

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.1077del (p.Ser362fs)	rs1555524370
NM_000546.6(TP53):c.1083del (p.Ser362fs)	rs1555524354
NM_000546.6(TP53):c.742C>T (p.Arg248Trp)	rs121912651

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