List of variants in gene FBXL4 reported as benign by Invitae

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_001278716.2(FBXL4):c.1569G>A (p.Gly523=)	rs11537982	0.06744
NM_001278716.2(FBXL4):c.465C>T (p.Leu155=)	rs1011676	0.05403
NM_001278716.2(FBXL4):c.105T>A (p.His35Gln)	rs34316889	0.02361
NM_001278716.2(FBXL4):c.978A>G (p.Gln326=)	rs61744041	0.00506
NM_001278716.2(FBXL4):c.429A>G (p.Leu143=)	rs17058965	0.00480
NM_001278716.2(FBXL4):c.1317+14A>G	rs182139048	0.00082
NM_001278716.2(FBXL4):c.468T>C (p.Ala156=)	rs114916821	0.00068
NM_001278716.2(FBXL4):c.1251A>G (p.Gln417=)	rs151258576	0.00043
NM_001278716.2(FBXL4):c.1703-36TGTTT[6]	rs377666976

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