Variants in gene FANCI with conflicting interpretations "uncertain significance" and "likely benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_001113378.2(FANCI):c.976-13A>T	rs145864790	0.00501
NM_001113378.2(FANCI):c.1573A>G (p.Met525Val)	rs144908351	0.00282
NM_001113378.2(FANCI):c.824T>C (p.Ile275Thr)	rs142906652	0.00071
NM_001113378.2(FANCI):c.1963G>A (p.Gly655Arg)	rs138026584	0.00019
NM_001113378.2(FANCI):c.2890-13C>T	rs377269890	0.00010
NM_001113378.2(FANCI):c.1699-11C>T	rs753750358	0.00003
NM_001113378.2(FANCI):c.1017G>A (p.Lys339=)	rs72762644	0.00001
NM_001113378.2(FANCI):c.1311A>G (p.Arg437=)	rs772846275	0.00001
NM_001113378.2(FANCI):c.2292-6T>C	rs772352819	0.00001
NM_001113378.2(FANCI):c.3721-7C>T	rs1434575390	0.00001
NM_001113378.2(FANCI):c.3059-11C>T	rs2054667046
NM_001113378.2(FANCI):c.669+17_669+18del	rs751881445

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