ClinVar Miner

List of variants in gene combination AOPEP, FANCC reported as likely benign by Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000136.3(FANCC):c.843+4C>T	rs4647506	0.01468
NM_000136.3(FANCC):c.584A>T (p.Asp195Val)	rs1800365	0.00275

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