ClinVar Miner

List of variants reported as uncertain significance for Fanconi anemia complementation group I by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001113378.2(FANCI):c.1537A>G (p.Met513Val)	rs148780626	0.00003
NM_001113378.2(FANCI):c.2687G>C (p.Gly896Ala)	rs751233975	0.00001
NM_001113378.2(FANCI):c.1240C>T (p.Pro414Ser)

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