C0238462[trait identifier] AND "CSER _CC_NCGL, University of Washingto - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 24881	NM_020975.6(RET):c.961G>A (p.Gly321Arg)	RET (G67R +2 more)	Single nucleotide variant (missense variant)	not provided +7 more	GConflicting classifications of pathogenicity
Select item 24883	NM_020975.6(RET):c.1531G>A (p.Glu511Lys)	RET (E257K +11 more)	Single nucleotide variant (missense variant)	not provided +5 more	GConflicting classifications of pathogenicity
Select item 24931	NM_020975.6(RET):c.1996A>G (p.Lys666Glu)	RET (K412E +13 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +7 more	GPathogenic/Likely pathogenic
Select item 13936	NM_020975.6(RET):c.2372A>T (p.Tyr791Phe)	RET (Y791F +17 more)	Single nucleotide variant (missense variant)	not provided +9 more	GBenign/Likely benign
Select item 24943	NM_020975.6(RET):c.2452G>A (p.Glu818Lys)	RET (E564K +16 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +6 more	GConflicting classifications of pathogenicity
Select item 24960	NM_020975.6(RET):c.2656C>T (p.Arg886Trp)	RET (R632W +16 more)	Single nucleotide variant (missense variant)	Renal hypoplasia/aplasia +3 more	GConflicting classifications of pathogenicity

ClinVar