ClinVar Miner

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

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Total variants: 17
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HGVS dbSNP
NM_000136.3(FANCC):c.*116A>C rs7048910
NM_000136.3(FANCC):c.*1288T>C rs4647554
NM_000136.3(FANCC):c.*1662C>T
NM_000136.3(FANCC):c.*1727T>A
NM_000136.3(FANCC):c.*1871G>A rs4647558
NM_000136.3(FANCC):c.*1968G>A rs114827984
NM_000136.3(FANCC):c.*2085C>A rs4647559
NM_000136.3(FANCC):c.*2552T>C rs9673
NM_000136.3(FANCC):c.*359A>G rs4647551
NM_000136.3(FANCC):c.*42G>A rs7029888
NM_000136.3(FANCC):c.-29A>C rs4647414
NM_000136.3(FANCC):c.-79+5G>A rs4647350
NM_000136.3(FANCC):c.1330-3C>T rs4647542
NM_000136.3(FANCC):c.1345G>A (p.Val449Met) rs1800367
NM_000136.3(FANCC):c.408A>G (p.Gln136=) rs1800360
NM_000136.3(FANCC):c.816C>T (p.Ile272=) rs55719336
NM_000136.3(FANCC):c.843+4C>T rs4647506

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