List of variants reported as uncertain significance for Li-Fraumeni syndrome by Illumina Laboratory Services, Illumina

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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.*346G>T	rs886053511
NM_000546.6(TP53):c.*347T>C	rs886053510
NM_000546.6(TP53):c.*382C>T	rs886053509
NM_000546.6(TP53):c.*548G>T	rs886053508
NM_000546.6(TP53):c.*565G>T	rs886053507
NM_000546.6(TP53):c.*735C>A	rs886053505
NM_000546.6(TP53):c.*747C>T	rs886053504
NM_000546.6(TP53):c.*772del	rs200757381
NM_000546.6(TP53):c.*779del	rs886053503
NM_000546.6(TP53):c.*806C>A	rs886053501
NM_000546.6(TP53):c.*977G>C	rs886053500
NM_000546.6(TP53):c.-73C>A	rs886053514
NM_000546.6(TP53):c.63C>T (p.Asp21=)	rs1800369

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