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

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (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.7362+62C>G	rs114497844	0.01054
NM_212482.4(FN1):c.6923T>C (p.Val2308Ala)	rs545761792	0.00120
NM_212482.4(FN1):c.7295G>C (p.Ser2432Thr)	rs147460086	0.00041

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