List of variants in gene combination FBXW4, LOC130004563 reported as benign for chromosomal disorder

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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_022039.4(FBXW4):c.461T>A (p.Val154Glu)	rs61382490	0.15406
NM_022039.4(FBXW4):c.534C>G (p.Ala178=)	rs61761937	0.03084
NM_022039.4(FBXW4):c.440C>A (p.Ala147Asp)	rs117664315	0.02439
NM_022039.4(FBXW4):c.472G>C (p.Ala158Pro)	rs111600818	0.01363

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