Variants in gene FN1 with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status:		Submission 1 (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_212482.4(FN1):c.4486C>T (p.Arg1496Trp)	rs139078629	0.00542
NM_212482.4(FN1):c.5435-7T>C	rs202045892	0.00068
NM_212482.4(FN1):c.6853+12C>G	rs111303746

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