C1968804[trait identifier] AND "Baylor Genetics"[submitter] - ClinVar

Format

Sort by

Choose Destination

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1032300	NM_000301.5(PLG):c.266G>C (p.Arg89Thr)	PLG (R89T)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 1029782	NM_000301.5(PLG):c.466G>A (p.Asp156Asn)	PLG (D156N)	Single nucleotide variant (missense variant)	Plasminogen deficiency, type I +1 more	GUncertain significance
Select item 692203	NM_000301.5(PLG):c.2045T>A (p.Ile682Asn)	PLG (I682N)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity

Format

Sort by

Choose Destination

ClinVar