ClinVar Miner

List of variants reported as uncertain significance for Fanconi anemia complementation group A by Institute of Human Genetics, Clinical Exome/Genome Diagnostics Group, University Hospital Bonn

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000135.4(FANCA):c.2859C>G (p.Asp953Glu)	rs149112292	0.00125
NM_000135.4(FANCA):c.1226-13G>A	rs377159744

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