List of variants in gene FANCI reported as benign by Sema4, Sema4

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001113378.2(FANCI):c.1114G>A (p.Val372Ile)	rs76788798	0.01679
NM_001113378.2(FANCI):c.1573A>G (p.Met525Val)	rs144908351	0.00282
NM_001113378.2(FANCI):c.286G>A (p.Glu96Lys)	rs149243307	0.00063
NM_001113378.2(FANCI):c.3051C>T (p.Asn1017=)	rs768378979	0.00016

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