List of variants reported as uncertain significance for Familial type 3 hyperlipoproteinemia

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000041.4(APOE):c.805C>G (p.Arg269Gly)	rs267606661	0.00031
NM_000041.4(APOE):c.882G>T (p.Trp294Cys)	rs557715042	0.00009
NM_000041.4(APOE):c.327dup (p.Arg110fs)	rs761350032
NM_000041.4(APOE):c.460C>T (p.Arg154Cys)

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