ClinVar Miner

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

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Total variants: 19
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HGVS dbSNP
NM_000136.3(FANCC):c.*1262T>C rs45520432
NM_000136.3(FANCC):c.*1516A>G rs541816451
NM_000136.3(FANCC):c.*1879C>T rs192262179
NM_000136.3(FANCC):c.*1895T>C rs56161090
NM_000136.3(FANCC):c.*213T>G
NM_000136.3(FANCC):c.*2164G>A
NM_000136.3(FANCC):c.*2271G>A rs562841213
NM_000136.3(FANCC):c.*250G>A
NM_000136.3(FANCC):c.*587C>T
NM_000136.3(FANCC):c.*593C>G rs561885351
NM_000136.3(FANCC):c.*5C>T rs117175949
NM_000136.3(FANCC):c.*660C>T
NM_000136.3(FANCC):c.-155A>C rs549658720
NM_000136.3(FANCC):c.1394A>G (p.Gln465Arg) rs1800368
NM_000136.3(FANCC):c.1407G>A (p.Thr469=) rs79722116
NM_000136.3(FANCC):c.1485G>A (p.Leu495=) rs56082100
NM_000136.3(FANCC):c.416G>A (p.Gly139Glu) rs1800362
NM_000136.3(FANCC):c.584A>T (p.Asp195Val) rs1800365
NM_000136.3(FANCC):c.973G>A (p.Ala325Thr) rs201407189

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