List of variants in gene combination FBXW4, LOC130004563 reported as uncertain significance for chromosome 10 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_022039.4(FBXW4):c.710G>A (p.Arg237Gln)	rs886046642	0.00001
NM_022039.4(FBXW4):c.409A>G (p.Arg137Gly)	rs886046645
NM_022039.4(FBXW4):c.437G>A (p.Trp146Ter)	rs886046644
NM_022039.4(FBXW4):c.493G>A (p.Glu165Lys)	rs886046643
NM_022039.4(FBXW4):c.507G>A (p.Ala169=)	rs1404824736
NM_022039.4(FBXW4):c.715G>A (p.Gly239Ser)	rs759941552

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