List of variants reported as likely pathogenic for hyperlipoproteinemia by Centogene AG - the Rare Disease Company

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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000237.3(LPL):c.1139+1G>A	rs767260655	0.00001
NM_000237.3(LPL):c.1160_1161insT (p.Lys387fs)	rs2070032216
NM_000237.3(LPL):c.784C>T (p.Gln262Ter)	rs1297688787

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