List of variants reported as likely pathogenic for familial lipoprotein lipase deficiency by Fulgent Genetics, Fulgent Genetics

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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_000237.3(LPL):c.998G>A (p.Arg333His)	rs144466625	0.00024
NM_000237.3(LPL):c.292G>A (p.Ala98Thr)	rs145657341	0.00006
NM_000237.3(LPL):c.755T>C (p.Ile252Thr)	rs118204080	0.00002
NM_000237.3(LPL):c.337T>C (p.Trp113Arg)	rs118204069	0.00001
NM_000237.3(LPL):c.590G>A (p.Arg197His)	rs372668179	0.00001
NM_000237.3(LPL):c.808C>T (p.Arg270Cys)	rs118204077	0.00001
NM_000237.3(LPL):c.1139+7A>G	rs2128839227
NM_000237.3(LPL):c.1187A>T (p.Glu396Val)	rs886037775
NM_000237.3(LPL):c.1242C>G (p.Tyr414Ter)
NM_000237.3(LPL):c.1373del (p.Ala458fs)
NM_000237.3(LPL):c.542-1G>A
NM_000237.3(LPL):c.663_670dup (p.Gln224fs)
NM_000237.3(LPL):c.679G>C (p.Val227Leu)
NM_000237.3(LPL):c.688del (p.Val230fs)	rs2128838185
NM_000237.3(LPL):c.802C>T (p.His268Tyr)

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