List of variants in gene FANCF reported as likely pathogenic for Fanconi anemia

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_022725.4(FANCF):c.690del (p.Gly231fs)	rs747622521	0.00001
NM_022725.4(FANCF):c.193C>T (p.Gln65Ter)	rs753272712
NM_022725.4(FANCF):c.1A>C (p.Met1Leu)	rs1046564488
NM_022725.4(FANCF):c.1A>T (p.Met1Leu)	rs1046564488

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