List of variants in gene combination FANCF, LOC130005444 reported as likely benign for DNA repair disease

Minimum submission review status:		Collection method:
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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.927T>C (p.Asn309=)	rs200073415	0.00001
NM_022725.4(FANCF):c.885T>G (p.Val295=)	rs761238804
NM_022725.4(FANCF):c.891T>G (p.Thr297=)	rs1060504373
NM_022725.4(FANCF):c.924C>T (p.His308=)

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