List of variants in gene SLFN13 reported as likely benign by Ambry Genetics

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_144682.6(SLFN13):c.2044A>G (p.Arg682Gly)	rs147476419	0.00013
NM_144682.6(SLFN13):c.1888G>A (p.Val630Ile)	rs537700636	0.00005
NM_144682.6(SLFN13):c.2150C>T (p.Pro717Leu)	rs778061533	0.00001
NM_144682.6(SLFN13):c.1015C>T (p.Arg339Cys)
NM_144682.6(SLFN13):c.1057G>A (p.Ala353Thr)	rs541429130
NM_144682.6(SLFN13):c.1321C>T (p.Leu441Phe)	rs552965029
NM_144682.6(SLFN13):c.1928G>A (p.Arg643Lys)
NM_144682.6(SLFN13):c.2089G>A (p.Val697Ile)
NM_144682.6(SLFN13):c.2260A>G (p.Ile754Val)
NM_144682.6(SLFN13):c.2501T>G (p.Met834Arg)
NM_144682.6(SLFN13):c.592A>C (p.Ile198Leu)	rs371819305
NM_144682.6(SLFN13):c.799G>A (p.Asp267Asn)	rs2509038230
NM_144682.6(SLFN13):c.872G>C (p.Arg291Pro)	rs776590437

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