Variants in gene NTRK1 with conflicting interpretations "pathogenic" and "likely pathogenic"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 21

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HGVS	dbSNP	gnomAD frequency
NM_002529.4(NTRK1):c.575-19G>A	rs370828525	0.00005
NM_002529.4(NTRK1):c.1354+1G>T	rs764771898	0.00003
NM_002529.4(NTRK1):c.2074C>T (p.Arg692Cys)	rs761967383	0.00002
NM_002529.4(NTRK1):c.1550G>A (p.Gly517Glu)	rs606231467	0.00001
NM_002529.4(NTRK1):c.2170G>A (p.Gly724Ser)	rs763122825	0.00001
NM_002529.4(NTRK1):c.2281C>T (p.Arg761Trp)	rs759637817	0.00001
NM_002529.4(NTRK1):c.2303C>T (p.Pro768Leu)	rs756981419	0.00001
NM_002529.4(NTRK1):c.2311C>T (p.Arg771Cys)	rs1324983370	0.00001
NM_002529.4(NTRK1):c.638T>C (p.Leu213Pro)	rs747711259	0.00001
NM_002529.4(NTRK1):c.1196-1G>A	rs764171953
NM_002529.4(NTRK1):c.1287C>A (p.Cys429Ter)	rs1647805941
NM_002529.4(NTRK1):c.1710_1738del (p.Gln570fs)
NM_002529.4(NTRK1):c.1729G>C (p.Gly577Arg)	rs121964866
NM_002529.4(NTRK1):c.1805G>A (p.Arg602Gln)	rs1647932465
NM_002529.4(NTRK1):c.2020G>T (p.Asp674Tyr)	rs80356677
NM_002529.4(NTRK1):c.2046dup (p.Val683fs)	rs2102925337
NM_002529.4(NTRK1):c.2084C>T (p.Pro695Leu)	rs121964868
NM_002529.4(NTRK1):c.2231del (p.Arg744fs)
NM_002529.4(NTRK1):c.359+5G>T	rs1571685765
NM_002529.4(NTRK1):c.360-2A>C	rs797045059
NM_002529.4(NTRK1):c.632T>A (p.Val211Glu)	rs1064793219

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