List of variants in gene CENPF reported as benign by CeGaT Center for Human Genetics Tuebingen

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_016343.4(CENPF):c.6984G>A (p.Glu2328=)	rs41277192	0.00505
NM_016343.4(CENPF):c.3369C>T (p.Ser1123=)	rs369791107	0.00001
NM_016343.4(CENPF):c.2101A>C (p.Met701Leu)	rs3795524

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