List of variants in gene combination INSRR, NTRK1 reported as uncertain significance for adenocarcinoma

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001007792.1(NTRK1):c.119C>A (p.Ala40Glu)	rs779943666	0.00003
NM_001007792.1(NTRK1):c.10-562dup	rs761392074	0.00001
NM_001007792.1(NTRK1):c.37del (p.Val13fs)	rs1451820799

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