List of variants in gene NTRK1 reported as likely pathogenic for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_002529.4(NTRK1):c.575-19G>A	rs370828525	0.00005
NM_002529.4(NTRK1):c.119_120insT (p.Cys41fs)	rs1131691595
NM_002529.4(NTRK1):c.1501+1G>A	rs1647858636
NM_002529.4(NTRK1):c.1501+5G>A	rs2102915746
NM_002529.4(NTRK1):c.1805G>A (p.Arg602Gln)	rs1647932465
NM_002529.4(NTRK1):c.1946G>A (p.Arg649Gln)	rs786205449
NM_002529.4(NTRK1):c.2092A>C (p.Ser698Arg)	rs2102927297
NM_002529.4(NTRK1):c.213-3C>A	rs2102885144
NM_002529.4(NTRK1):c.359+5G>T	rs1571685765
NM_002529.4(NTRK1):c.632T>A (p.Val211Glu)	rs1064793219

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