List of variants in gene NTRK2 reported as likely pathogenic for obesity, hyperphagia, and developmental delay

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_006180.6(NTRK2):c.1279G>T (p.Gly427Cys)	rs142393662
NM_006180.6(NTRK2):c.1651C>T (p.Arg551Ter)
NM_006180.6(NTRK2):c.1652G>A (p.Arg551Gln)
NM_006180.6(NTRK2):c.2164T>G (p.Tyr722Asp)

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