List of variants in gene DNAAF2 reported as benign by PreventionGenetics, part of Exact Sciences

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_018139.3(DNAAF2):c.1864-40G>T	rs2985696	0.71001
NM_018139.3(DNAAF2):c.186G>C (p.Glu62Asp)	rs2985684	0.65918
NM_018139.3(DNAAF2):c.498C>T (p.Ala166=)	rs2985685	0.65889
NM_018139.3(DNAAF2):c.1482A>G (p.Thr494=)	rs2985687	0.65543
NM_018139.3(DNAAF2):c.1863+16A>G	rs60822508	0.01613
NM_018139.3(DNAAF2):c.707C>T (p.Pro236Leu)	rs74050429	0.01450
NM_018139.3(DNAAF2):c.78C>T (p.Ala26=)	rs7156297	0.01255
NM_018139.3(DNAAF2):c.144C>A (p.Asn48Lys)	rs116185352	0.01062
NM_018139.3(DNAAF2):c.1367C>T (p.Pro456Leu)	rs137991407	0.00785
NM_018139.3(DNAAF2):c.728A>C (p.Glu243Ala)	rs112044935	0.00642
NM_018139.3(DNAAF2):c.1494G>A (p.Ser498=)	rs2985688	0.00470
NM_018139.3(DNAAF2):c.1406G>A (p.Cys469Tyr)	rs150737854	0.00410
NM_018139.3(DNAAF2):c.1851C>T (p.Asn617=)	rs147090213	0.00373
NM_018139.3(DNAAF2):c.1953A>G (p.Pro651=)	rs34352773	0.00287
NM_018139.3(DNAAF2):c.2176A>G (p.Thr726Ala)	rs80237479	0.00088
NM_018139.3(DNAAF2):c.1463G>A (p.Gly488Glu)	rs200121200	0.00052

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