List of variants in gene combination AOPEP, FANCC reported as likely benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_000136.3(FANCC):c.1156T>C (p.Ser386Pro)	rs41281202	0.00236
NM_000136.3(FANCC):c.934A>G (p.Ile312Val)	rs1800366	0.00051
NM_000136.3(FANCC):c.1533+50G>A	rs4647544	0.00046
NM_000136.3(FANCC):c.672C>T (p.Asn224=)	rs150647141	0.00046
NM_000136.3(FANCC):c.705C>T (p.Pro235=)	rs141828876	0.00046
NM_000136.3(FANCC):c.1509G>A (p.Thr503=)	rs144278080	0.00011
NM_000136.3(FANCC):c.609C>T (p.Leu203=)	rs567226063	0.00006
NM_000136.3(FANCC):c.1425A>G (p.Thr475=)	rs199739450	0.00005
NM_000136.3(FANCC):c.1494T>C (p.Ala498=)	rs76895298	0.00005
NM_000136.3(FANCC):c.1560C>T (p.His520=)	rs150020474	0.00005
NM_000136.3(FANCC):c.1414G>A (p.Gly472Arg)	rs201063698	0.00002
NM_000136.3(FANCC):c.1485G>A (p.Leu495=)	rs56082100

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