List of variants reported as likely benign for Fanconi anemia complementation group C by Fulgent Genetics, Fulgent Genetics

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Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_000136.3(FANCC):c.843+4C>T	rs4647506	0.01468
NM_000136.3(FANCC):c.457-18A>G	rs377206543	0.00036
NM_000136.3(FANCC):c.-78-18T>G	rs560839822	0.00032
NM_000136.3(FANCC):c.1534-9T>C	rs536836859	0.00011
NM_000136.3(FANCC):c.250+16G>A	rs371993188	0.00011
NM_000136.3(FANCC):c.251-20T>C	rs370867462	0.00009
NM_000136.3(FANCC):c.1533+13G>A	rs200515307	0.00008
NM_000136.3(FANCC):c.1330-6G>T	rs1223668739	0.00003
NM_000136.3(FANCC):c.165+17A>G	rs1046183823	0.00002
NM_000136.3(FANCC):c.1534-18C>T	rs1289718209	0.00001
NM_000136.3(FANCC):c.166-9C>G	rs372507085	0.00001
NM_000136.3(FANCC):c.687-15A>C	rs765327075	0.00001
NM_000136.3(FANCC):c.1485G>A (p.Leu495=)	rs56082100
NM_000136.3(FANCC):c.1503C>T (p.Gly501=)	rs2134454633
NM_000136.3(FANCC):c.843+12G>A	rs2135164340
NM_000136.3(FANCC):c.896+14T>C	rs2134966492

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