List of variants reported as benign for Fanconi anemia complementation group C by Illumina Laboratory Services, Illumina

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Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_000136.3(FANCC):c.*1288T>C	rs4647554	0.45294
NM_000136.3(FANCC):c.*1871G>A	rs4647558	0.36840
NM_000136.3(FANCC):c.*116A>C	rs7048910	0.03439
NM_000136.3(FANCC):c.*2552T>C	rs9673	0.02750
NM_000136.3(FANCC):c.408A>G (p.Gln136=)	rs1800360	0.02397
NM_000136.3(FANCC):c.1345G>A (p.Val449Met)	rs1800367	0.02254
NM_000136.3(FANCC):c.*2085C>A	rs4647559	0.01780
NM_000136.3(FANCC):c.*359A>G	rs4647551	0.01505
NM_000136.3(FANCC):c.843+4C>T	rs4647506	0.01468
NM_000136.3(FANCC):c.1330-3C>T	rs4647542	0.00811
NM_000136.3(FANCC):c.-79+5G>A	rs4647350	0.00411
NM_000136.3(FANCC):c.*1968G>A	rs114827984	0.00409
NM_000136.3(FANCC):c.-29A>C	rs4647414	0.00155
NM_000136.3(FANCC):c.816C>T (p.Ile272=)	rs55719336	0.00074
NM_000136.3(FANCC):c.*1662C>T	rs4647556
NM_000136.3(FANCC):c.*1727T>A	rs4647557
NM_000136.3(FANCC):c.*42G>A	rs7029888

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