Related gene-specific medical variations for Gene (Select 1117) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3144343	NM_004000.3(CHI3L2):c.424G>A (p.Val142Ile)	CHI3L2, LOC126805828 (V132I +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3144342	NM_004000.3(CHI3L2):c.330G>A (p.Gly110=)	CHI3L2, LOC126805828	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2588531	NM_004000.3(CHI3L2):c.386T>C (p.Ile129Thr)	CHI3L2, LOC126805828 (I129T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389734	NM_004000.3(CHI3L2):c.518C>T (p.Ser173Phe)	CHI3L2, LOC126805828 (S163F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 769524	NM_004000.3(CHI3L2):c.550G>A (p.Val184Ile)	CHI3L2, LOC126805828 (V105I +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 546606	NM_004000.3(CHI3L2):c.1159del (p.Gly388fs)	CHI3L2 (G388fs +2 more)	Deletion (frameshift variant)	not provided	GUncertain significance

ClinVar