C1704981[trait identifier] AND "CSER _CC_NCGL, University of Washingto - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 226036	NM_003783.3(B3GALT2):c.367T>G (p.Tyr123Asp)	B3GALT2, CDC73 (Y123D)	Single nucleotide variant (missense variant +1 more)	Hyperparathyroidism 2 with jaw tumors	GLikely benign
Select item 21681	NM_024529.5(CDC73):c.1066+8T>C	CDC73	Single nucleotide variant (intron variant)	Hyperparathyroidism 2 with jaw tumors +2 more	GLikely benign