ClinVar for MedGen (Select 1780930) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2664052	NM_001009606.4(HS3ST6):c.946C>G (p.Leu316Val)	HS3ST6 (L316V)	Single nucleotide variant (missense variant)	Angioedema, hereditary, 8	GUncertain significance
Select item 1162308	NM_001009606.4(HS3ST6):c.430A>T (p.Thr144Ser)	HS3ST6 (T144S)	Single nucleotide variant (missense variant)	Angioedema, hereditary, 8	GPathogenic