List of variants in gene FANCF reported as likely benign by Genetic Services Laboratory, University of Chicago

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_022725.4(FANCF):c.246C>T (p.Asn82=)	rs139724351	0.00185
NM_022725.4(FANCF):c.687A>T (p.Ser229=)	rs776140806	0.00021
NM_022725.4(FANCF):c.465A>T (p.Pro155=)	rs201215734	0.00020
NM_022725.4(FANCF):c.350C>T (p.Pro117Leu)	rs374572943	0.00010
NM_022725.4(FANCF):c.279C>T (p.Leu93=)	rs199578614	0.00002
NM_022725.4(FANCF):c.807G>A (p.Ala269=)	rs754312601	0.00001
NM_022725.4(FANCF):c.345C>A (p.Leu115=)	rs749884571
NM_022725.4(FANCF):c.774G>A (p.Gly258=)	rs2133796823

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