List of variants in gene FBXL4 reported as benign by GeneDx

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: 18

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HGVS	dbSNP	gnomAD frequency
NM_001278716.2(FBXL4):c.-130C>A	rs195812	0.69264
NM_001278716.2(FBXL4):c.1318-230C>T	rs195831	0.69057
NM_001278716.2(FBXL4):c.1103+30T>C	rs6935315	0.36921
NM_001278716.2(FBXL4):c.1702+291_1702+292insA	rs5878565	0.36901
NM_001278716.2(FBXL4):c.512+298G>A	rs1011674	0.36801
NM_001278716.2(FBXL4):c.1389+222T>C	rs2281123	0.15288
NM_001278716.2(FBXL4):c.1703-37G>A	rs3765239	0.15264
NM_001278716.2(FBXL4):c.1317+209C>G	rs58270328	0.13857
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.512+294G>A	rs112341850	0.01986
NM_001278716.2(FBXL4):c.*3T>C	rs115180578	0.01773
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.*5A>G	rs142988015	0.00361
NM_001278716.2(FBXL4):c.468T>C (p.Ala156=)	rs114916821	0.00068
NM_001278716.2(FBXL4):c.512+173T>G	rs1011675

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