ClinVar Miner

List of variants reported as pathogenic for Fanconi anemia complementation group C by Laboratory of Medical Genetics, National & Kapodistrian University of Athens

Included ClinVar conditions (1):

Fanconi anemia complementation group C

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Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000136.3(FANCC):c.166-2A>G	rs587777945	0.00001
NM_000136.3(FANCC):c.844-1G>C	rs774209201	0.00001

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