List of variants reported as likely pathogenic for Fanconi anemia complementation group C by Revvity Omics, Revvity

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000136.3(FANCC):c.1533+1G>C	rs753885687	0.00001
NM_000136.3(FANCC):c.1628C>A (p.Ser543Ter)	rs867319477	0.00001
NM_000136.3(FANCC):c.124C>T (p.Gln42Ter)
NM_000136.3(FANCC):c.2T>C (p.Met1Thr)	rs2136102345
NM_000136.3(FANCC):c.494_495del (p.His165fs)	rs1564719151

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