List of variants in gene combination LOC126862483, TP53, WRAP53 reported as uncertain significance for Li-Fraumeni syndrome

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_000546.5(TP53):c.-202_-29+?dup174
NM_000546.6(TP53):c.-29+1G>A	rs2151082372
NM_000546.6(TP53):c.-29+1G>C	rs2151082372
NM_000546.6(TP53):c.-29+1G>T	rs2151082372
NM_000546.6(TP53):c.-73C>A	rs886053514

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