List of variants in gene FBXW4 reported as likely benign for chromosomal disorder

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_022039.4(FBXW4):c.134C>T (p.Ala45Val)	rs557225276	0.00351
NM_022039.4(FBXW4):c.*453C>T	rs570558261	0.00263
NM_022039.4(FBXW4):c.*233G>T	rs535051082	0.00231
NM_022039.4(FBXW4):c.*204G>A	rs185181909	0.00040
NM_022039.4(FBXW4):c.353G>A (p.Gly118Glu)	rs532195262	0.00031
NM_022039.4(FBXW4):c.1235+13T>G	rs193073481	0.00024
NM_022039.4(FBXW4):c.755T>C (p.Val252Ala)	rs143070839	0.00021
NM_022039.4(FBXW4):c.*3G>A	rs777074009	0.00005
NM_022039.4(FBXW4):c.1254G>A (p.Thr418=)	rs142870264	0.00002
NM_022039.4(FBXW4):c.1437C>T (p.Ser479=)	rs574963392	0.00001
NM_022039.4(FBXW4):c.822-11C>T	rs540055383

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