C4748657[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1464436	NM_018965.4(TREM2):c.486C>G (p.Ser162Arg)	TREM2 (S162R)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 196494	NM_018965.4(TREM2):c.469C>T (p.His157Tyr)	TREM2 (H157Y)	Single nucleotide variant (missense variant)	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2 +2 more	GBenign/Likely benign
Select item 1517663	NM_018965.4(TREM2):c.451G>A (p.Glu151Lys)	TREM2 (E151K)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 502024	NM_018965.4(TREM2):c.292C>T (p.Arg98Trp)	TREM2 (R98W)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 195350	NM_018965.4(TREM2):c.140G>A (p.Arg47His)	TREM2 (R47H)	Single nucleotide variant (missense variant)	not specified +2 more	GLikely benign
Select item 356682	NM_018965.4(TREM2):c.-51G>A	TREM2	Single nucleotide variant	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2	GUncertain significance
Select item 906413	NM_018965.4(TREM2):c.-98C>T	TREM2	Single nucleotide variant	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2	GUncertain significance

ClinVar