List of variants in gene combination FANCF, LOC130005443 reported as benign for hematologic disorder

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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: 2

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HGVS	dbSNP	gnomAD frequency
NM_022725.4(FANCF):c.959C>T (p.Pro320Leu)	rs45451294	0.01158
NM_022725.4(FANCF):c.970A>G (p.Lys324Glu)	rs200416138	0.00008

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