C1835407[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1384148	NM_002838.5(PTPRC):c.248C>T (p.Thr83Ile)	PTPRC (T83I)	Single nucleotide variant (missense variant +1 more)	Immunodeficiency 104 +2 more	GUncertain significance
Select item 1085729	NM_002838.5(PTPRC):c.596A>G (p.Asn199Ser)	PTPRC (N199S +1 more)	Single nucleotide variant (missense variant)	Immunodeficiency 104 +1 more	GLikely benign
Select item 440228	NM_002838.5(PTPRC):c.982A>G (p.Ile328Val)	PTPRC (I328V +1 more)	Single nucleotide variant (missense variant)	Immunodeficiency 104 +2 more	GUncertain significance
Select item 378445	NM_002838.5(PTPRC):c.1052A>G (p.Asn351Ser)	PTPRC (N351S +1 more)	Single nucleotide variant (missense variant)	not specified +3 more	GBenign/Likely benign
Select item 1290650	NM_002838.5(PTPRC):c.2848-4del	PTPRC	Deletion (intron variant)	Hepatitis C virus, susceptibility to +2 more	GBenign
Select item 516877	NM_002838.5(PTPRC):c.2848-5_2848-4del	PTPRC	Deletion (intron variant)	Immunodeficiency 104 +2 more	GBenign
Select item 190992	NM_002838.5(PTPRC):c.3545T>C (p.Leu1182Ser)	PTPRC (L1182S +1 more)	Single nucleotide variant (missense variant)	Immunodeficiency 104 +4 more	GConflicting classifications of pathogenicity

ClinVar