"Illumina Laboratory Services, Illumina"[submitter] AND "LPL"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 362397	NM_000237.2(LPL):c.-299T>G	LPL	Single nucleotide variant	Hyperlipoproteinemia, type I	GUncertain significance
Select item 362398	NM_000237.3(LPL):c.-283G>T	LPL	Single nucleotide variant	not provided +1 more	GConflicting classifications of pathogenicity
Select item 362399	NM_000237.2(LPL):c.-281T>G	LPL	Single nucleotide variant	Hyperlipoproteinemia, type I +1 more	GBenign
Select item 362400	NM_000237.3(LPL):c.-172_-171dup	LPL	Duplication (5 prime UTR variant)	Hyperlipoproteinemia, type I +1 more	GConflicting classifications of pathogenicity
Select item 362401	NM_000237.3(LPL):c.-136T>C	LPL	Single nucleotide variant (5 prime UTR variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 911585	NM_000237.3(LPL):c.-101C>T	LPL	Single nucleotide variant (5 prime UTR variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 362402	NM_000237.3(LPL):c.-71C>G	LPL	Single nucleotide variant (5 prime UTR variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 362403	NM_000237.3(LPL):c.-49C>T	LPL	Single nucleotide variant (5 prime UTR variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 362404	NM_000237.3(LPL):c.-38C>G	LPL	Single nucleotide variant (5 prime UTR variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 908632	NM_000237.3(LPL):c.36C>A (p.Ala12=)	LPL	Single nucleotide variant (synonymous variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 908633	NM_000237.3(LPL):c.81C>A (p.Ala27=)	LPL	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +2 more	GConflicting classifications of pathogenicity
Select item 1552	NM_000237.3(LPL):c.106G>A (p.Asp36Asn)	LPL (D36N)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +4 more	GBenign/Likely benign; other
Select item 755163	NM_000237.3(LPL):c.112G>A (p.Glu38Lys)	LPL (E38K)	Single nucleotide variant (missense variant)	Hyperlipoproteinemia, type I +3 more	GConflicting classifications of pathogenicity
Select item 908634	NM_000237.3(LPL):c.134C>A (p.Thr45Asn)	LPL (T45N)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 764668	NM_000237.3(LPL):c.189C>T (p.Ser63=)	LPL	Single nucleotide variant (synonymous variant)	Hyperlipoproteinemia, type I +4 more	GConflicting classifications of pathogenicity
Select item 908635	NM_000237.3(LPL):c.249G>A (p.Thr83=)	LPL	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 362405	NM_000237.3(LPL):c.260T>C (p.Met87Thr)	LPL (M87T)	Single nucleotide variant (missense variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 723310	NM_000237.3(LPL):c.290C>T (p.Ala97Val)	LPL (A97V)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 362406	NM_000237.3(LPL):c.333G>T (p.Val111=)	LPL	Single nucleotide variant (synonymous variant)	Hyperlipoproteinemia, type I +2 more	GConflicting classifications of pathogenicity
Select item 719805	NM_000237.3(LPL):c.345A>C (p.Ser115=)	LPL	Single nucleotide variant (synonymous variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 362407	NM_000237.3(LPL):c.405G>A (p.Val135=)	LPL	Single nucleotide variant (synonymous variant)	Hyperlipoproteinemia, type I +2 more	GBenign
Select item 362408	NM_000237.3(LPL):c.430-6C>T	LPL	Single nucleotide variant (intron variant)	Hyperlipoproteinemia, type I +1 more	GBenign/Likely benign
Select item 362409	NM_000237.3(LPL):c.435G>A (p.Glu145=)	LPL	Single nucleotide variant (synonymous variant)	Hyperlipoproteinemia, type I +2 more	GBenign
Select item 909490	NM_000237.3(LPL):c.439A>C (p.Asn147His)	LPL (N147H)	Single nucleotide variant (missense variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 721152	NM_000237.3(LPL):c.456T>C (p.Asn152=)	LPL	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign/Likely benign
Select item 362410	NM_000237.3(LPL):c.478C>T (p.Leu160Phe)	LPL (L160F)	Single nucleotide variant (missense variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 910420	NM_000237.3(LPL):c.501T>C (p.Ile167=)	LPL	Single nucleotide variant (synonymous variant)	Hyperlipoproteinemia, type I +1 more	GConflicting classifications of pathogenicity
Select item 747870	NM_000237.3(LPL):c.528C>G (p.Val176=)	LPL	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +2 more	GConflicting classifications of pathogenicity
Select item 910421	NM_000237.3(LPL):c.648C>T (p.Ser216=)	LPL	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1529	NM_000237.3(LPL):c.662T>C (p.Ile221Thr)	LPL (I221T)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +3 more	GConflicting classifications of pathogenicity
Select item 362411	NM_000237.3(LPL):c.678A>G (p.Pro226=)	LPL	Single nucleotide variant (synonymous variant)	Hyperlipoproteinemia, type I +2 more	GBenign/Likely benign
Select item 742198	NM_000237.3(LPL):c.687T>C (p.His229=)	LPL	Single nucleotide variant (synonymous variant)	LPL-related condition +4 more	GConflicting classifications of pathogenicity
Select item 362412	NM_000237.3(LPL):c.786G>A (p.Gln262=)	LPL	Single nucleotide variant (synonymous variant)	Hyperlipoproteinemia, type I +4 more	GConflicting classifications of pathogenicity
Select item 1550	NM_000237.3(LPL):c.953A>G (p.Asn318Ser)	LPL (N318S)	Single nucleotide variant (missense variant)	Hyperlipidemia, familial combined, LPL related +4 more	GConflicting classifications of pathogenicity
Select item 632073	NM_000237.3(LPL):c.998G>A (p.Arg333His)	LPL (R333H)	Single nucleotide variant (missense variant)	Hyperlipoproteinemia, type I +3 more	GConflicting classifications of pathogenicity
Select item 495741	NM_000237.3(LPL):c.1135A>G (p.Thr379Ala)	LPL (T379A)	Single nucleotide variant (missense variant)	Hyperlipoproteinemia, type I +4 more	GBenign/Likely benign
Select item 495742	NM_000237.3(LPL):c.1136C>T (p.Thr379Ile)	LPL (T379I)	Single nucleotide variant (missense variant)	Hyperlipoproteinemia, type I +3 more	GConflicting classifications of pathogenicity
Select item 362413	NM_000237.3(LPL):c.1164C>A (p.Thr388=)	LPL	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign
Select item 911648	NM_000237.3(LPL):c.1196T>C (p.Ile399Thr)	LPL (I399T)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 362414	NM_000237.3(LPL):c.1279G>A (p.Ala427Thr)	LPL (A427T)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +3 more	GBenign/Likely benign
Select item 766071	NM_000237.3(LPL):c.1325T>G (p.Val442Gly)	LPL (V442G)	Single nucleotide variant (missense variant)	not specified +5 more	GConflicting classifications of pathogenicity
Select item 911649	NM_000237.3(LPL):c.1373C>T (p.Ala458Val)	LPL (A458V)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 362415	NM_000237.3(LPL):c.1416_1417insT (p.Lys473Ter)	LPL (K473*)	Insertion (nonsense)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 1534	NM_000237.3(LPL):c.1421C>G (p.Ser474Ter)	LPL (S474*)	Single nucleotide variant (nonsense)	Cardiovascular phenotype +5 more	GBenign
Select item 908696	NM_000237.3(LPL):c.1427+15C>A	LPL	Single nucleotide variant (intron variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 362416	NM_000237.3(LPL):c.*8C>T	LPL	Single nucleotide variant (3 prime UTR variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 362417	NM_000237.3(LPL):c.*9G>A	LPL	Single nucleotide variant (3 prime UTR variant)	not provided +1 more	GBenign
Select item 908697	NM_000237.3(LPL):c.*29G>A	LPL	Single nucleotide variant (3 prime UTR variant)	Hyperlipoproteinemia, type I	GBenign
Select item 908698	NM_000237.3(LPL):c.*135C>A	LPL	Single nucleotide variant (3 prime UTR variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 908699	NM_000237.3(LPL):c.*221C>T	LPL	Single nucleotide variant (3 prime UTR variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 362418	NM_000237.3(LPL):c.*222A>C	LPL	Single nucleotide variant (3 prime UTR variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 362419	NM_000237.3(LPL):c.*262G>A	LPL	Single nucleotide variant (3 prime UTR variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 362420	NM_000237.3(LPL):c.290_293del	LPL	Deletion (3 prime UTR variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 362421	NM_000237.3(LPL):c.*309A>T	LPL	Single nucleotide variant (3 prime UTR variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 362422	NM_000237.3(LPL):c.*371T>C	LPL	Single nucleotide variant (3 prime UTR variant)	not provided +1 more	GBenign
Select item 909552	NM_000237.3(LPL):c.*389C>G	LPL	Single nucleotide variant (3 prime UTR variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 362423	NM_000237.3(LPL):c.414_418del	LPL	Deletion (3 prime UTR variant)	Hyperlipoproteinemia, type I +1 more	GConflicting classifications of pathogenicity
Select item 362424	NM_000237.3(LPL):c.*448C>T	LPL	Single nucleotide variant (3 prime UTR variant)	Hyperlipoproteinemia, type I	GLikely benign
Select item 909553	NM_000237.3(LPL):c.*455C>A	LPL	Single nucleotide variant (3 prime UTR variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 362425	NM_000237.3(LPL):c.*544A>G	LPL	Single nucleotide variant (3 prime UTR variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 909554	NM_000237.3(LPL):c.*547T>C	LPL	Single nucleotide variant (3 prime UTR variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 909555	NM_000237.3(LPL):c.*648A>T	LPL	Single nucleotide variant (3 prime UTR variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 362426	NM_000237.3(LPL):c.*677T>C	LPL	Single nucleotide variant (3 prime UTR variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 362427	NM_000237.3(LPL):c.*688G>A	LPL	Single nucleotide variant (3 prime UTR variant)	Hyperlipoproteinemia, type I	GLikely benign
Select item 910482	NM_000237.3(LPL):c.*729A>G	LPL	Single nucleotide variant (3 prime UTR variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 362428	NM_000237.3(LPL):c.*796A>G	LPL	Single nucleotide variant (3 prime UTR variant)	Hyperlipoproteinemia, type I	GBenign
Select item 362429	NM_000237.3(LPL):c.*824dup	LPL	Duplication (3 prime UTR variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 362430	NM_000237.3(LPL):c.*827A>T	LPL	Single nucleotide variant (3 prime UTR variant)	not provided +1 more	GBenign
Select item 910483	NM_000237.3(LPL):c.*831G>A	LPL	Single nucleotide variant (3 prime UTR variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 362431	NM_000237.3(LPL):c.*846G>C	LPL	Single nucleotide variant (3 prime UTR variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 362432	NM_000237.3(LPL):c.*853C>T	LPL	Single nucleotide variant (3 prime UTR variant)	Hyperlipoproteinemia, type I	GBenign
Select item 362433	NM_000237.3(LPL):c.*884A>C	LPL	Single nucleotide variant (3 prime UTR variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 911713	NM_000237.3(LPL):c.*903C>T	LPL	Single nucleotide variant (3 prime UTR variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 362434	NM_000237.3(LPL):c.*949G>A	LPL	Single nucleotide variant (3 prime UTR variant)	Hyperlipoproteinemia, type I	GBenign
Select item 362435	NM_000237.3(LPL):c.*1039G>A	LPL	Single nucleotide variant (3 prime UTR variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 911714	NM_000237.3(LPL):c.*1048A>C	LPL	Single nucleotide variant (3 prime UTR variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 362436	NM_000237.3(LPL):c.*1142C>T	LPL	Single nucleotide variant (3 prime UTR variant)	not provided +1 more	GBenign
Select item 362437	NM_000237.3(LPL):c.*1159C>T	LPL	Single nucleotide variant (3 prime UTR variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 362438	NM_000237.3(LPL):c.*1167C>A	LPL	Single nucleotide variant (3 prime UTR variant)	not provided +1 more	GLikely benign
Select item 362439	NM_000237.3(LPL):c.*1214G>T	LPL	Single nucleotide variant (3 prime UTR variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 362440	NM_000237.3(LPL):c.*1224C>A	LPL	Single nucleotide variant (3 prime UTR variant)	not provided +1 more	GBenign
Select item 362441	NM_000237.3(LPL):c.*1250A>G	LPL	Single nucleotide variant (3 prime UTR variant)	not provided +1 more	GBenign
Select item 362442	NM_000237.3(LPL):c.*1279G>A	LPL	Single nucleotide variant (3 prime UTR variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 362443	NM_000237.3(LPL):c.*1291G>A	LPL	Single nucleotide variant (3 prime UTR variant)	Hyperlipoproteinemia, type I	GBenign
Select item 362444	NM_000237.3(LPL):c.*1308G>C	LPL	Single nucleotide variant (3 prime UTR variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 908758	NM_000237.3(LPL):c.*1373G>A	LPL	Single nucleotide variant (3 prime UTR variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 908759	NM_000237.3(LPL):c.*1387T>C	LPL	Single nucleotide variant (3 prime UTR variant)	Hyperlipoproteinemia, type I	GLikely benign
Select item 909611	NM_000237.3(LPL):c.*1394A>C	LPL	Single nucleotide variant (3 prime UTR variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 909612	NM_000237.3(LPL):c.*1399G>A	LPL	Single nucleotide variant (3 prime UTR variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 909613	NM_000237.3(LPL):c.*1414C>T	LPL	Single nucleotide variant (3 prime UTR variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 362445	NM_000237.3(LPL):c.*1416T>C	LPL	Single nucleotide variant (3 prime UTR variant)	Hyperlipoproteinemia, type I	GBenign
Select item 909614	NM_000237.3(LPL):c.*1547T>A	LPL	Single nucleotide variant (3 prime UTR variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 362446	NM_000237.3(LPL):c.1563_1567del	LPL	Deletion (3 prime UTR variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 362447	NM_000237.3(LPL):c.*1660G>A	LPL	Single nucleotide variant (3 prime UTR variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 40131	NM_000237.3(LPL):c.*1671T>C	LPL	Single nucleotide variant (3 prime UTR variant)	not provided +1 more	GBenign
Select item 362448	NM_000237.3(LPL):c.*1742T>C	LPL	Single nucleotide variant (3 prime UTR variant)	not provided +1 more	GBenign
Select item 910542	NM_000237.3(LPL):c.*1743G>A	LPL	Single nucleotide variant (3 prime UTR variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 910543	NM_000237.3(LPL):c.*1749T>C	LPL	Single nucleotide variant (3 prime UTR variant)	Hyperlipoproteinemia, type I	GUncertain significance
Select item 362449	NM_000237.3(LPL):c.*1783A>T	LPL	Single nucleotide variant (3 prime UTR variant)	Hyperlipoproteinemia, type I	GBenign
Select item 910544	NM_000237.3(LPL):c.*1788T>C	LPL	Single nucleotide variant (3 prime UTR variant)	Hyperlipoproteinemia, type I	GUncertain significance

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