C1833921[trait identifier] AND "KCCC/NGS Laboratory, Kuwait Cancer Con - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 132713	NM_020975.6(RET):c.1264-5C>T	RET	Single nucleotide variant (intron variant)	Familial medullary thyroid carcinoma +10 more	GBenign/Likely benign
Select item 13911	NM_020975.6(RET):c.1901G>T (p.Cys634Phe)	RET (C634F +14 more)	Single nucleotide variant (missense variant)	not provided +3 more	GPathogenic
Select item 219833	NM_020975.6(RET):c.2393-9C>T	RET	Single nucleotide variant (intron variant)	Multiple endocrine neoplasia, type 2 +6 more	GBenign/Likely benign
Select item 37102	NM_020975.6(RET):c.2410G>A (p.Val804Met)	RET (V804M +17 more)	Single nucleotide variant (missense variant)	RET-related condition +13 more	GPathogenic/Likely pathogenic
Select item 13951	NM_020975.6(RET):c.2671T>G (p.Ser891Ala)	RET (S891A +17 more)	Single nucleotide variant (missense variant)	Pheochromocytoma +10 more	GPathogenic
Select item 13938	NM_020975.6(RET):c.2944C>T (p.Arg982Cys)	RET (R982C +17 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +11 more	GConflicting classifications of pathogenicity

ClinVar