ClinVar Miner

List of variants reported as benign 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.3651+19G>A	rs73472624	0.01789
NM_001113378.2(FANCI):c.3525C>A (p.Ala1175=)	rs114810692	0.00625
NM_001113378.2(FANCI):c.2997C>T (p.Ser999=)	rs138675752	0.00248

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