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

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001007792.1(NTRK1):c.163C>A (p.Arg55Ser)	rs543320028	0.00004
NM_002529.4(NTRK1):c.219C>T (p.Ile73=)	rs563296138	0.00003
NM_002529.4(NTRK1):c.2143G>A (p.Val715Met)	rs759190964	0.00001
NM_002529.4(NTRK1):c.2312G>A (p.Arg771His)	rs780724170	0.00001
NM_002529.4(NTRK1):c.1946G>A (p.Arg649Gln)	rs786205449

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