C3151303[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1574065	NM_006180.6(NTRK2):c.288-15T>C	NTRK2	Single nucleotide variant (intron variant)	Obesity, hyperphagia, and developmental delay +2 more	GBenign/Likely benign
Select item 1148855	NM_006180.6(NTRK2):c.500C>A (p.Ser167Tyr)	NTRK2 (S11Y +1 more)	Single nucleotide variant (missense variant)	not provided +4 more	GLikely benign
Select item 1599583	NM_006180.6(NTRK2):c.1396+10del	NTRK2	Deletion (intron variant)	Obesity, hyperphagia, and developmental delay +2 more	GBenign/Likely benign
Select item 1515143	NM_006180.6(NTRK2):c.1549G>A (p.Val517Ile)	NTRK2 (V361I +4 more)	Single nucleotide variant (missense variant)	Obesity, hyperphagia, and developmental delay +3 more	GUncertain significance
Select item 722021	NM_006180.6(NTRK2):c.1962G>A (p.Leu654=)	NTRK2	Single nucleotide variant (synonymous variant)	Developmental and epileptic encephalopathy, 58 +3 more	GLikely benign
Select item 285265	NM_006180.6(NTRK2):c.2113C>T (p.Leu705=)	NTRK2	Single nucleotide variant (synonymous variant)	Obesity, hyperphagia, and developmental delay +3 more	GBenign/Likely benign
Select item 285975	NM_006180.6(NTRK2):c.2430C>T (p.Pro810=)	NTRK2	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign/Likely benign
Select item 728564	NM_006180.6(NTRK2):c.2478G>A (p.Leu826=)	NTRK2	Single nucleotide variant (synonymous variant)	not specified +3 more	GLikely benign

ClinVar