Variants in gene combination LOC129931648, NTRK1 with conflicting interpretations reported as "likely benign and "uncertain significance"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_002529.4(NTRK1):c.16C>T (p.Arg6Trp)	rs201472270	0.00373
NM_002529.4(NTRK1):c.10G>A (p.Gly4Ser)	rs556840308	0.00173
NM_002529.4(NTRK1):c.12C>T (p.Gly4=)	rs757229319	0.00001

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