List of variants reported as benign for Fanconi anemia complementation group C

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Total variants: 28

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HGVS	dbSNP	gnomAD frequency
NM_000136.3(FANCC):c.1155-38T>C	rs4647534	0.48457
NM_000136.3(FANCC):c.*1288T>C	rs4647554	0.45294
NM_000136.3(FANCC):c.521+109A>G	rs3737142	0.37815
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.416G>A (p.Gly139Glu)	rs1800362	0.01494
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.77C>T (p.Ser26Phe)	rs1800361	0.00511
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.1329+175C>T	rs112446681	0.00401
NM_000136.3(FANCC):c.1394A>G (p.Gln465Arg)	rs1800368	0.00361
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.457-18A>G	rs377206543	0.00036
NM_000136.3(FANCC):c.973G>A (p.Ala325Thr)	rs201407189	0.00028
NM_000136.3(FANCC):c.1509G>A (p.Thr503=)	rs144278080	0.00011
NM_000136.3(FANCC):c.251-20T>C	rs370867462	0.00009
NM_000136.3(FANCC):c.*1662C>T	rs4647556
NM_000136.3(FANCC):c.*1727T>A	rs4647557
NM_000136.3(FANCC):c.*42G>A	rs7029888
NM_000136.3(FANCC):c.1485G>A (p.Leu495=)	rs56082100

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