Variants in gene FANCI with conflicting interpretations "pathogenic" and "likely pathogenic"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) 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: 15

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HGVS	dbSNP	gnomAD frequency
NM_001113378.2(FANCI):c.3041G>A (p.Cys1014Tyr)	rs140404896	0.00011
NM_001113378.2(FANCI):c.1461T>A (p.Tyr487Ter)	rs769248873	0.00005
NM_001113378.2(FANCI):c.3622_3623del (p.Leu1208fs)	rs1491132258	0.00003
NM_001113378.2(FANCI):c.2422A>T (p.Lys808Ter)	rs375656231	0.00001
NM_001113378.2(FANCI):c.2509G>T (p.Glu837Ter)	rs748000458	0.00001
NM_001113378.2(FANCI):c.2568_2569del (p.Gly857fs)	rs1385885533	0.00001
NM_001113378.2(FANCI):c.3006+3A>G	rs1294973649	0.00001
NM_001113378.2(FANCI):c.3058+1G>A	rs149464307	0.00001
NM_001113378.2(FANCI):c.158-2A>G	rs762128147
NM_001113378.2(FANCI):c.2345_2346del (p.Leu781_Ser782insTer)	rs758062617
NM_001113378.2(FANCI):c.2737C>T (p.Gln913Ter)	rs1359408831
NM_001113378.2(FANCI):c.295del (p.His99fs)	rs759398314
NM_001113378.2(FANCI):c.3493del (p.Asp1165fs)	rs758597713
NM_001113378.2(FANCI):c.3626_3627del (p.Cys1209fs)	rs770318990
NM_001113378.2(FANCI):c.849T>A (p.Tyr283Ter)	rs760412752

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