List of variants in gene NTRK1 reported as likely benign by Natera, Inc.

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: 19

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HGVS	dbSNP	gnomAD frequency
NM_002529.4(NTRK1):c.1236C>T (p.Asp412=)	rs147438950	0.00289
NM_002529.4(NTRK1):c.612G>A (p.Ser204=)	rs114320051	0.00251
NM_002529.4(NTRK1):c.865C>A (p.Gln289Lys)	rs137979116	0.00118
NM_002529.4(NTRK1):c.315C>T (p.Phe105=)	rs6340	0.00031
NM_002529.4(NTRK1):c.505G>A (p.Gly169Arg)	rs367836863	0.00030
NM_002529.4(NTRK1):c.927G>A (p.Pro309=)	rs144015813	0.00018
NM_002529.4(NTRK1):c.375C>T (p.Asn125=)	rs757803799	0.00005
NM_002529.4(NTRK1):c.1902C>T (p.Val634=)	rs148270992	0.00004
NM_002529.4(NTRK1):c.1029C>T (p.His343=)	rs772855825	0.00003
NM_002529.4(NTRK1):c.1083G>T (p.Leu361=)	rs750656916	0.00003
NM_002529.4(NTRK1):c.321G>A (p.Ala107=)	rs774351278	0.00002
NM_002529.4(NTRK1):c.1020C>T (p.Thr340=)	rs781390842	0.00001
NM_002529.4(NTRK1):c.675C>T (p.Ala225=)	rs1407589933	0.00001
NM_002529.4(NTRK1):c.879G>A (p.Ala293=)	rs766259168	0.00001
NM_002529.4(NTRK1):c.102A>G (p.Ala34=)	rs2102879190
NM_002529.4(NTRK1):c.1080G>T (p.Thr360=)	rs2274498
NM_002529.4(NTRK1):c.1395C>T (p.Ser465=)	rs1311708647
NM_002529.4(NTRK1):c.618T>C (p.Asp206=)	rs1571690231
NM_002529.4(NTRK1):c.792G>A (p.Thr264=)	rs201110800

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