List of variants reported as uncertain significance for Fanconi anemia complementation group C by Mendelics

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000136.3(FANCC):c.843+5G>A	rs369082921	0.00006
NM_000136.3(FANCC):c.28T>G (p.Cys10Gly)	rs147479204	0.00004
NM_000136.3(FANCC):c.871T>C (p.Phe291Leu)	rs769649289	0.00001
NM_000136.3(FANCC):c.202G>A (p.Gly68Ser)	rs777111154
NM_000136.3(FANCC):c.413T>G (p.Leu138Arg)	rs1564720454

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