C1704981[trait identifier] AND "KCCC/NGS Laboratory, Kuwait Cancer Con - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 294408	NM_024529.5(CDC73):c.-95G>A	CDC73	Single nucleotide variant (5 prime UTR variant)	Hyperparathyroidism 1 +2 more	GBenign/Likely benign
Select item 21680	NM_024529.5(CDC73):c.-11G>A	CDC73	Single nucleotide variant (5 prime UTR variant)	Hyperparathyroidism +3 more	GConflicting classifications of pathogenicity
Select item 1231125	NM_024529.5(CDC73):c.237+28T>C	CDC73	Single nucleotide variant (intron variant)	Hyperparathyroidism 2 with jaw tumors +1 more	GBenign
Select item 241498	NM_024529.5(CDC73):c.840G>A (p.Leu280=)	CDC73	Single nucleotide variant (synonymous variant)	CDC73-related disorder +4 more	GLikely benign
Select item 412622	NM_024529.5(CDC73):c.1011C>T (p.Ala337=)	CDC73	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +4 more	GConflicting classifications of pathogenicity
Select item 241491	NM_024529.5(CDC73):c.1185A>G (p.Gln395=)	CDC73	Single nucleotide variant (synonymous variant)	Parathyroid carcinoma +5 more	GBenign/Likely benign
Select item 21682	NM_024529.5(CDC73):c.1418-17C>G	CDC73	Single nucleotide variant (intron variant)	not provided +3 more	GBenign

ClinVar