List of variants in gene FANCI reported as pathogenic for not provided

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_001113378.2(FANCI):c.1461T>A (p.Tyr487Ter)	rs769248873	0.00005
NM_001113378.2(FANCI):c.3853C>T (p.Arg1285Ter)	rs121918164	0.00005
NM_001113378.2(FANCI):c.1597C>T (p.Arg533Ter)	rs1347292940	0.00001
NM_001113378.2(FANCI):c.2509G>T (p.Glu837Ter)	rs748000458	0.00001
NM_001113378.2(FANCI):c.3493del (p.Asp1165fs)	rs758597713
NM_001113378.2(FANCI):c.3720+1G>A
NM_001113378.2(FANCI):c.3801_3804del (p.Ser1268fs)	rs2152017390
NM_001113378.2(FANCI):c.3895C>T (p.Arg1299Ter)	rs551305056
NM_001113378.2(FANCI):c.85-1656_157+358del

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