List of variants reported as pathogenic for hyperlipoproteinemia by Clinical Genomics Laboratory, Stanford Medicine

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000527.5(LDLR):c.429C>A (p.Cys143Ter)	rs199774121	0.00001
NM_000527.4:c.(?_-1)_(940+1_941-1)del
NM_000527.5(LDLR):c.1897C>T (p.Arg633Cys)

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