"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "LPL"[ge - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 362399	NC_000008.11:g.19939160T>G	LPL	Single nucleotide variant	not provided +1 more	GBenign
Select item 763853	NC_000008.11:g.19939200G>C	LPL	Single nucleotide variant	not specified +1 more	GConflicting classifications of pathogenicity
Select item 362400	NM_000237.3(LPL):c.-172_-171dup	LPL	Duplication (5 prime UTR variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2006935	NM_000237.3(LPL):c.3G>A (p.Met1Ile)	LPL (M1I)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely pathogenic
Select item 1941573	NM_000237.3(LPL):c.6G>A (p.Glu2=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1455947	NM_000237.3(LPL):c.10_19del (p.Lys4fs)	LPL (K4fs)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 1149017	NM_000237.3(LPL):c.9C>T (p.Ser3=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1118542	NM_000237.3(LPL):c.15C>G (p.Ala5=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1095681	NM_000237.3(LPL):c.15C>A (p.Ala5=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 763630	NM_000237.3(LPL):c.15C>T (p.Ala5=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2830448	NM_000237.3(LPL):c.18G>T (p.Leu6=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1787583	NM_000237.3(LPL):c.21C>A (p.Leu7=)	LPL	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1728789	NM_000237.3(LPL):c.31C>T (p.Leu11=)	LPL	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 1560072	NM_000237.3(LPL):c.33G>T (p.Leu11=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2153588	NM_000237.3(LPL):c.35C>T (p.Ala12Val)	LPL (A12V)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 1735058	NM_000237.3(LPL):c.37G>T (p.Val13Leu)	LPL (V13L)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 643218	NM_000237.3(LPL):c.41G>A (p.Trp14Ter)	LPL (W14*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 2754564	NM_000237.3(LPL):c.45C>T (p.Leu15=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1646511	NM_000237.3(LPL):c.45C>G (p.Leu15=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1431010	NM_000237.3(LPL):c.46_47del (p.Gln16fs)	LPL (Q16fs)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 2040146	NM_000237.3(LPL):c.52C>T (p.Leu18=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2919886	NM_000237.3(LPL):c.57C>T (p.Thr19=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1999761	NM_000237.3(LPL):c.57C>G (p.Thr19=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 796201	NM_000237.3(LPL):c.57C>A (p.Thr19=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 753489	NM_000237.3(LPL):c.59C>T (p.Ala20Val)	LPL (A20V)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1085341	NM_000237.3(LPL):c.60C>T (p.Ala20=)	LPL	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 1654202	NM_000237.3(LPL):c.63C>T (p.Ser21=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2089784	NM_000237.3(LPL):c.69A>G (p.Gly23=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1143682	NM_000237.3(LPL):c.72G>C (p.Gly24=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
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 991263	NM_000237.3(LPL):c.84C>G (p.Ala28=)	LPL	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 2823414	NM_000237.3(LPL):c.88+1del	LPL	Deletion (splice donor variant)	not provided	GLikely pathogenic
Select item 2735123	NM_000237.3(LPL):c.88+2dup	LPL	Duplication (splice donor variant)	not provided	GPathogenic
Select item 1639811	NM_000237.3(LPL):c.88+9T>C	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1131983	NM_000237.3(LPL):c.88+10G>A	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2838150	NM_000237.3(LPL):c.88+12G>A	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2796222	NM_000237.3(LPL):c.88+14G>C	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1991684	NM_000237.3(LPL):c.88+16A>G	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2991949	NM_000237.3(LPL):c.89-19del	LPL	Deletion (intron variant)	not provided	GLikely benign
Select item 3015165	NM_000237.3(LPL):c.89-17C>T	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3014470	NM_000237.3(LPL):c.89-15A>T	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 495745	NM_000237.3(LPL):c.89-10del	LPL	Deletion (intron variant)	not provided +1 more	GBenign
Select item 1566200	NM_000237.3(LPL):c.89-10T>C	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2845491	NM_000237.3(LPL):c.89-9C>G	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 740136	NM_000237.3(LPL):c.89-9C>T	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1087610	NM_000237.3(LPL):c.89-7T>G	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1113542	NM_000237.3(LPL):c.89-4C>A	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1494261	NM_000237.3(LPL):c.89-1G>A	LPL	Single nucleotide variant (splice acceptor variant)	not provided	GLikely pathogenic
Select item 1492400	NM_000237.3(LPL):c.89-1G>C	LPL	Single nucleotide variant (splice acceptor variant)	not provided	GLikely pathogenic
Select item 950321	NM_000237.3(LPL):c.94_98del (p.Arg32fs)	LPL (R32fs)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 2011344	NM_000237.3(LPL):c.102T>C (p.Phe34=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1155293	NM_000237.3(LPL):c.105C>T (p.Ile35=)	LPL	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 1080124	NM_000237.3(LPL):c.105C>A (p.Ile35=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1552	NM_000237.3(LPL):c.106G>A (p.Asp36Asn)	LPL (D36N)	Single nucleotide variant (missense variant)	not specified +3 more	GBenign/Likely benign; other
Select item 1656680	NM_000237.3(LPL):c.108C>T (p.Asp36=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 796133	NM_000237.3(LPL):c.111C>T (p.Ile37=)	LPL	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +2 more	GLikely benign
Select item 755163	NM_000237.3(LPL):c.112G>A (p.Glu38Lys)	LPL (E38K)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +3 more	GConflicting classifications of pathogenicity
Select item 1134564	NM_000237.3(LPL):c.123T>C (p.Phe41=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2793081	NM_000237.3(LPL):c.127dup (p.Leu43fs)	LPL (L43fs)	Duplication (frameshift variant)	not provided	GPathogenic
Select item 1972479	NM_000237.3(LPL):c.126C>T (p.Ala42=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 908634	NM_000237.3(LPL):c.134C>A (p.Thr45Asn)	LPL (T45N)	Single nucleotide variant (missense variant)	not specified +2 more	GUncertain significance
Select item 2863398	NM_000237.3(LPL):c.135C>A (p.Thr45=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1399464	NM_000237.3(LPL):c.138del (p.Glu47fs)	LPL (E47fs)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 2805844	NM_000237.3(LPL):c.141A>G (p.Glu47=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2863224	NM_000237.3(LPL):c.147del (p.Ala50fs)	LPL (A50fs)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 1774819	NM_000237.3(LPL):c.153G>A (p.Glu51=)	LPL	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1087226	NM_000237.3(LPL):c.162C>T (p.Cys54=)	LPL	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 1147258	NM_000237.3(LPL):c.174C>T (p.Pro58=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 764668	NM_000237.3(LPL):c.189C>T (p.Ser63=)	LPL	Single nucleotide variant (synonymous variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 1782856	NM_000237.3(LPL):c.192G>C (p.Val64=)	LPL	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1113688	NM_000237.3(LPL):c.192G>A (p.Val64=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1978374	NM_000237.3(LPL):c.206T>C (p.Phe69Ser)	LPL (F69S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2769182	NM_000237.3(LPL):c.214_224del (p.Ser72fs)	LPL (S72fs)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 1100360	NM_000237.3(LPL):c.213C>T (p.His71=)	LPL	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 495743	NM_000237.3(LPL):c.213C>G (p.His71Gln)	LPL (H71Q)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign/Likely benign
Select item 2764196	NM_000237.3(LPL):c.216C>T (p.Ser72=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1667368	NM_000237.3(LPL):c.225C>G (p.Thr75=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2051211	NM_000237.3(LPL):c.234G>C (p.Val78=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1552345	NM_000237.3(LPL):c.240T>C (p.His80=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1535	NM_000237.3(LPL):c.249+1G>A	LPL	Single nucleotide variant (splice donor variant)	Cardiovascular phenotype +2 more	GPathogenic
Select item 2727830	NM_000237.3(LPL):c.249+9G>A	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2980267	NM_000237.3(LPL):c.249+17G>A	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2738219	NM_000237.3(LPL):c.249+19G>A	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2852240	NM_000237.3(LPL):c.250-20G>A	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2738496	NM_000237.3(LPL):c.250-19C>T	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2149043	NM_000237.3(LPL):c.250-17del	LPL	Deletion (intron variant)	not provided	GUncertain significance
Select item 2917907	NM_000237.3(LPL):c.250-16G>T	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2829717	NM_000237.3(LPL):c.250-16G>A	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2895318	NM_000237.3(LPL):c.250-14G>A	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2139675	NM_000237.3(LPL):c.250-8_250-6del	LPL	Microsatellite (intron variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 1097417	NM_000237.3(LPL):c.250-8A>G	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2828376	NM_000237.3(LPL):c.250-7T>C	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1132346	NM_000237.3(LPL):c.250-6C>T	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2843115	NM_000237.3(LPL):c.250-2A>C	LPL	Single nucleotide variant (splice acceptor variant)	not provided	GLikely pathogenic
Select item 1666276	NM_000237.3(LPL):c.252A>T (p.Val84=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1124365	NM_000237.3(LPL):c.264T>C (p.Tyr88=)	LPL	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 1558443	NM_000237.3(LPL):c.267G>A (p.Glu89=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1113208	NM_000237.3(LPL):c.270T>C (p.Ser90=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1541	NM_000237.3(LPL):c.272G>A (p.Trp91Ter)	LPL (W91*)	Single nucleotide variant (nonsense)	not provided +1 more	GPathogenic
Select item 765755	NM_000237.3(LPL):c.276G>A (p.Val92=)	LPL	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign

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