ClinVar Miner

List of variants reported as likely pathogenic for Fanconi anemia complementation group C by Natera, Inc.

Included ClinVar conditions (1):

Fanconi anemia complementation group C

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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.843+1G>A	rs587779909	0.00002
NM_000136.3(FANCC):c.996+1G>T	rs370510954	0.00001
NM_000136.3(FANCC):c.996+1G>A	rs370510954

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