Related gene-specific medical variations for Gene (Select 146723) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3140531	NM_001115152.2(CD300LD):c.-11G>A	CD300LD, CD300LD-AS1 +1 more	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3140526	NM_001115152.2(CD300LD):c.166G>A (p.Ala56Thr)	CD300LD, CD300LD-AS1 (A56T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2648225	NM_001115152.2(CD300LD):c.285G>A (p.Glu95=)	CD300LD, CD300LD-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2519683	NM_001115152.2(CD300LD):c.280A>G (p.Met94Val)	CD300LD, CD300LD-AS1 (M94V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2471115	NM_001115152.2(CD300LD):c.97G>A (p.Gly33Ser)	CD300LD, CD300LD-AS1 (G33S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304284	NM_001115152.2(CD300LD):c.169G>A (p.Asp57Asn)	CD300LD, CD300LD-AS1 (D57N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar