C2717906[trait identifier] AND "Genome-Nilou Lab"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 254785	NM_000062.3(SERPING1):c.1030-20A>G	SERPING1	Single nucleotide variant (intron variant)	Hereditary angioedema type 1 +2 more	GBenign
Select item 254786	NM_000062.3(SERPING1):c.1438G>A (p.Val480Met)	SERPING1 (V480M)	Single nucleotide variant (missense variant)	Hereditary angioedema type 1 +3 more	GBenign