List of variants in gene TP53 reported as likely benign by True Health Diagnostics

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.639A>G (p.Arg213=)	rs1800372	0.01238
NM_000546.6(TP53):c.108G>A (p.Pro36=)	rs1800370	0.00974
NM_000546.6(TP53):c.97-6C>T	rs35117667	0.00785
NM_000546.6(TP53):c.885T>C (p.Pro295=)	rs200073907	0.00001
NM_000546.6(TP53):c.789T>C (p.Asn263=)	rs770598448

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