ClinVar Miner

List of variants reported as uncertain significance for Fanconi anemia complementation group A by Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000135.4(FANCA):c.437C>G (p.Ser146Cys)	rs141367100	0.00042
NM_000135.4(FANCA):c.2187C>A (p.Asn729Lys)
NM_000135.4(FANCA):c.2994T>G (p.Tyr998Ter)

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