C1858680[trait identifier] AND "Revvity Omics, Revvity"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 534956	NM_001122752.2(SERPINI1):c.248A>T (p.Asn83Ile)	SERPINI1 (N83I)	Single nucleotide variant (missense variant)	Familial encephalopathy with neuroserpin inclusion bodies	GUncertain significance
Select item 2435818	NM_001122752.2(SERPINI1):c.863T>C (p.Val288Ala)	SERPINI1 (V288A)	Single nucleotide variant (missense variant)	Familial encephalopathy with neuroserpin inclusion bodies	GUncertain significance