List of variants in gene CENPF reported as 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_016343.4(CENPF):c.3623C>T (p.Ala1208Val)	rs114717799	0.00986
NM_016343.4(CENPF):c.1145G>A (p.Arg382Lys)	rs114338555	0.00540
NM_016343.4(CENPF):c.7753G>A (p.Val2585Met)	rs62636591	0.00473
NM_016343.4(CENPF):c.7544A>C (p.Gln2515Pro)	rs62636593	0.00437
NM_016343.4(CENPF):c.6550G>A (p.Val2184Ile)	rs62623663	0.00435
NM_016343.4(CENPF):c.562T>C (p.Leu188=)	rs61732049	0.00364
NM_016343.4(CENPF):c.2271T>C (p.His757=)	rs111676558	0.00333
NM_016343.4(CENPF):c.4470G>A (p.Leu1490=)	rs112985127	0.00332
NM_016343.4(CENPF):c.2101A>C (p.Met701Leu)	rs3795524

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