Variants in gene combination FN1, FN1-DT with conflicting interpretations reported as "benign and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) 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_212482.4(FN1):c.56C>T (p.Thr19Ile)	rs143438305	0.00859
NM_212482.4(FN1):c.40G>C (p.Val14Leu)	rs115937626	0.00370
NM_212482.4(FN1):c.54G>C (p.Gly18=)	rs149268490	0.00096

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