List of variants reported as pathogenic for Fanconi anemia complementation group I by Fulgent Genetics, Fulgent Genetics

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001113378.2(FANCI):c.2345_2346del (p.Leu781_Ser782insTer)	rs758062617
NM_001113378.2(FANCI):c.3493del (p.Asp1165fs)	rs758597713
NM_001113378.2(FANCI):c.3626_3627del (p.Cys1209fs)	rs770318990

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