List of variants in gene FANCC reported as benign by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 22

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HGVS	dbSNP	gnomAD frequency
NM_000136.3(FANCC):c.-79+19952A>C	rs4647376	0.72347
NM_000136.3(FANCC):c.521+109A>G	rs3737142	0.37815
NM_000136.3(FANCC):c.250+220G>A	rs356667	0.18637
NM_000136.3(FANCC):c.-78-262T>C	rs4647412	0.03550
NM_000136.3(FANCC):c.-79+24854T>C	rs73539228	0.02502
NM_000136.3(FANCC):c.408A>G (p.Gln136=)	rs1800360	0.02397
NM_000136.3(FANCC):c.416G>A (p.Gly139Glu)	rs1800362	0.01494
NM_000136.3(FANCC):c.77C>T (p.Ser26Phe)	rs1800361	0.00511
NM_000136.3(FANCC):c.-29A>C	rs4647414	0.00155
NM_000136.3(FANCC):c.457-18A>G	rs377206543	0.00036
NM_000136.3(FANCC):c.166-7T>C	rs369052148	0.00027
NM_000136.3(FANCC):c.-79+7G>T	rs551170090	0.00019
NM_000136.3(FANCC):c.251-20T>C	rs370867462	0.00009
NM_000136.3(FANCC):c.457-7T>C	rs749994612	0.00002
NM_000136.3(FANCC):c.-87G>A	rs1051113986	0.00001
NM_000136.3(FANCC):c.15A>G (p.Ser5=)	rs778408360	0.00001
NM_000136.3(FANCC):c.166-9C>G	rs372507085	0.00001
NM_000136.3(FANCC):c.468A>G (p.Ser156=)	rs148616725	0.00001
NM_000136.3(FANCC):c.132C>T (p.Phe44=)	rs2136100617
NM_000136.3(FANCC):c.250+196AC[13]	rs3030679
NM_000136.3(FANCC):c.250+196AC[14]	rs3030679
NM_000136.3(FANCC):c.345+4AG[2]	rs755657969

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