C2717906[trait identifier] AND "Institute of Human Genetics, Universit - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 976258	NM_000062.3(SERPING1):c.1193T>C (p.Leu398Pro)	SERPING1 (L398P)	Single nucleotide variant (missense variant)	Hereditary angioedema type 1	GLikely pathogenic
Select item 3947	NM_000062.3(SERPING1):c.1396C>T (p.Arg466Cys)	SERPING1 (R466C)	Single nucleotide variant (missense variant)	not provided +1 more	GPathogenic