CN068920[trait identifier] AND "Rady Children's Institute for Genomic - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 128042	NM_007194.4(CHEK2):c.1100del (p.Thr367fs)	CHEK2 (T146fs +4 more)	Deletion (frameshift variant)	Malignant tumor of prostate +18 more	GPathogenic
Select item 128075	NM_007194.4(CHEK2):c.444+1G>A	CHEK2	Single nucleotide variant (splice donor variant)	Li-Fraumeni syndrome 2 +14 more	GPathogenic/Likely pathogenic
Select item 141866	NM_007194.4(CHEK2):c.279G>A (p.Trp93Ter)	CHEK2 (W93*)	Single nucleotide variant (nonsense +1 more)	Hereditary breast ovarian cancer syndrome +5 more	GPathogenic/Likely pathogenic

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ClinVar