List of variants in gene FBXL4 reported as likely 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: 19

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HGVS	dbSNP	gnomAD frequency
NM_001278716.2(FBXL4):c.1103+140T>C	rs72627757	0.01653
NM_001278716.2(FBXL4):c.1103+29T>C	rs189497833	0.01110
NM_001278716.2(FBXL4):c.1389+184G>A	rs150045568	0.01103
NM_001278716.2(FBXL4):c.*90G>C	rs111226417	0.00576
NM_001278716.2(FBXL4):c.1317+264G>A	rs141987023	0.00396
NM_001278716.2(FBXL4):c.1104-126T>A	rs550657550	0.00376
NM_001278716.2(FBXL4):c.*9A>G	rs185850413	0.00127
NM_001278716.2(FBXL4):c.-69A>G	rs144837535	0.00112
NM_001278716.2(FBXL4):c.1317+14A>G	rs182139048	0.00082
NM_001278716.2(FBXL4):c.-79A>G	rs574428980	0.00043
NM_001278716.2(FBXL4):c.1251A>G (p.Gln417=)	rs151258576	0.00043
NM_001278716.2(FBXL4):c.351G>A (p.Thr117=)	rs375173811	0.00018
NM_001278716.2(FBXL4):c.1389+23T>C	rs182295874	0.00010
NM_001278716.2(FBXL4):c.1566C>T (p.Thr522=)	rs149704398	0.00008
NM_001278716.2(FBXL4):c.273T>C (p.Phe91=)	rs1438963021	0.00001
NM_001278716.2(FBXL4):c.1103+30del	rs377101732
NM_001278716.2(FBXL4):c.1353A>G (p.Ser451=)	rs141165629
NM_001278716.2(FBXL4):c.1703-36TGTTT[6]	rs377666976
NM_001278716.2(FBXL4):c.702T>C (p.Leu234=)	rs1554221171

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