ClinVar Miner

List of variants in gene combination FANCI, POLG reported as likely benign for Fanconi anemia complementation group I

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001113378.2(FANCI):c.3816+15A>T	rs28493988	0.02368
NM_002693.3(POLG):c.3644-72C>A	rs1801377	0.00312

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