List of variants in gene combination AOPEP, FANCC reported as benign by CeGaT Center for Human Genetics Tuebingen

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000136.3(FANCC):c.*96A>G	rs55687573	0.00893
NM_000136.3(FANCC):c.816C>T (p.Ile272=)	rs55719336	0.00074
NM_000136.3(FANCC):c.*5C>T	rs117175949	0.00033

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