Variants in gene FANCI 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_001113378.2(FANCI):c.2487T>G (p.Leu829=)	rs145762491	0.00155
NM_001113378.2(FANCI):c.1856T>A (p.Leu619Gln)	rs151038616	0.00011
NM_001113378.2(FANCI):c.3816+17_3816+19del	rs374324314

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