ClinVar for Gene (Select 4023) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3068354	NM_000237.3(LPL):c.1127_1137del (p.Ile376fs)	LPL (I376fs)	Deletion (frameshift variant)	Hyperlipidemia, familial combined, LPL related	GPathogenic
Select item 3066297	NM_000237.3(LPL):c.386_389del (p.Lys129fs)	LPL (K129fs)	Deletion (frameshift variant)	Hyperlipidemia, familial combined, LPL related	GLikely pathogenic
Select item 3063027	GRCh37/hg19 8p23.3-11.21(chr8:158048-41600696)x3	DEFB134, DEFB135 +234 more	Copy number gain	not specified	GPathogenic
Select item 3063013	GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)x3	AARD, ABRA +665 more	Copy number gain	not specified	GPathogenic
Select item 3020967	NM_000237.3(LPL):c.541+18T>C	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3017837	NM_000237.3(LPL):c.870G>A (p.Arg290=)	LPL	Single nucleotide variant (synonymous 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 3010890	NM_000237.3(LPL):c.1113C>G (p.Ala371=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3010646	NM_000237.3(LPL):c.900G>T (p.Gly300=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3006722	NM_000237.3(LPL):c.684G>A (p.Gly228=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3006226	NM_000237.3(LPL):c.1139+16G>A	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3006057	NM_000237.3(LPL):c.333G>A (p.Val111=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3004006	NM_000237.3(LPL):c.776-7dup	LPL	Duplication (intron variant)	not provided	GBenign
Select item 3003133	NM_000237.3(LPL):c.378C>A (p.Gly126=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2999253	NM_000237.3(LPL):c.1428-18T>C	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2992928	NM_000237.3(LPL):c.568G>A (p.Glu190Lys)	LPL (E190K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2992733	NM_000237.3(LPL):c.1019-1G>A	LPL	Single nucleotide variant (splice acceptor variant)	not provided	GLikely pathogenic
Select item 2991949	NM_000237.3(LPL):c.89-19del	LPL	Deletion (intron variant)	not provided	GLikely benign
Select item 2988969	NM_000237.3(LPL):c.1018+12A>G	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2988064	NM_000237.3(LPL):c.305G>C (p.Arg102Thr)	LPL (R102T)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic
Select item 2988045	NM_000237.3(LPL):c.828C>A (p.Ile276=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2985254	NM_000237.3(LPL):c.732C>T (p.Asn244=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2985224	NM_000237.3(LPL):c.1140-14G>A	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2982831	NM_000237.3(LPL):c.1427+20del	LPL	Deletion (intron variant)	not provided	GLikely benign
Select item 2982060	NM_000237.3(LPL):c.1019-13T>C	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 2978890	NM_000237.3(LPL):c.363C>T (p.Tyr121=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2977369	NM_000237.3(LPL):c.1427+8T>A	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2976096	NM_000237.3(LPL):c.1139+12A>T	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2972813	NM_000237.3(LPL):c.1014C>G (p.Tyr338Ter)	LPL (Y338*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 2965680	NM_000237.3(LPL):c.534A>G (p.Arg178=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2964606	NM_000237.3(LPL):c.1427+14G>A	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2963632	NM_000237.3(LPL):c.775+15G>A	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2959112	NM_000237.3(LPL):c.1427+13G>A	LPL	Single nucleotide variant (intron 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 2918791	NM_000237.3(LPL):c.1428-12_1428-11insT	LPL	Insertion (intron variant)	not provided	GLikely benign
Select item 2917907	NM_000237.3(LPL):c.250-16G>T	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2916109	NM_000237.3(LPL):c.542-18_542-16del	LPL	Deletion (intron variant)	not provided	GLikely benign
Select item 2913183	NM_000237.3(LPL):c.1019-18G>A	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2912842	NM_000237.3(LPL):c.1139+14G>A	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2910502	NM_000237.3(LPL):c.1139+14G>T	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2909073	NM_000237.3(LPL):c.429+13G>A	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2906107	NM_000237.3(LPL):c.1139+13G>C	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2902929	NM_000237.3(LPL):c.450G>A (p.Leu150=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2901077	NM_000237.3(LPL):c.429+11G>A	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2895548	NM_000237.3(LPL):c.429+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 2894781	NM_000237.3(LPL):c.776-17G>A	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2894160	NM_000237.3(LPL):c.1139+15G>A	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2885431	NM_000237.3(LPL):c.775+20G>A	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2884875	NM_000237.3(LPL):c.541+16C>T	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2879905	NM_000237.3(LPL):c.498C>T (p.Gly166=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2876937	NM_000237.3(LPL):c.1323-9C>T	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2874984	NM_000237.3(LPL):c.366A>G (p.Pro122=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2872828	NM_000237.3(LPL):c.541+8A>G	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2867283	NM_000237.3(LPL):c.1161G>A (p.Lys387=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2867006	NM_000237.3(LPL):c.1266C>T (p.Ser422=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2863975	NM_000237.3(LPL):c.1322+11G>A	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2863398	NM_000237.3(LPL):c.135C>A (p.Thr45=)	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 2862787	NM_000237.3(LPL):c.705T>C (p.Asn235=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2852632	NM_000237.3(LPL):c.1074C>A (p.Thr358=)	LPL	Single nucleotide variant (synonymous 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 2850186	NM_000237.3(LPL):c.573T>C (p.Tyr191=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2849043	NM_000237.3(LPL):c.538del (p.Thr180fs)	LPL (T180fs)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 2845491	NM_000237.3(LPL):c.89-9C>G	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2844695	NM_000237.3(LPL):c.1323-14A>G	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2843825	NM_000237.3(LPL):c.542-13T>A	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 2840731	NM_000237.3(LPL):c.1187_1188del (p.Glu396fs)	LPL (E396fs)	Microsatellite (frameshift variant)	not provided	GPathogenic
Select item 2840369	NM_000237.3(LPL):c.1019-10T>C	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 2837811	NM_000237.3(LPL):c.591T>C (p.Arg197=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2834920	NM_000237.3(LPL):c.776-19G>A	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2834432	NM_000237.3(LPL):c.1139+16_1139+30del	LPL	Deletion (intron 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 2830347	NM_000237.3(LPL):c.776-15C>G	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2830102	NM_000237.3(LPL):c.1341G>A (p.Arg447=)	LPL	Single nucleotide variant (synonymous 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 2828376	NM_000237.3(LPL):c.250-7T>C	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2825737	NM_000237.3(LPL):c.1071T>C (p.His357=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2823414	NM_000237.3(LPL):c.88+1del	LPL	Deletion (splice donor variant)	not provided	GLikely pathogenic
Select item 2821358	NM_000237.3(LPL):c.594T>A (p.Leu198=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2814855	NM_000237.3(LPL):c.573T>G (p.Tyr191Ter)	LPL (Y191*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 2812348	NM_000237.3(LPL):c.987C>T (p.Tyr329=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2805844	NM_000237.3(LPL):c.141A>G (p.Glu47=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2805746	NM_000237.3(LPL):c.1019-12C>A	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2805687	NM_000237.3(LPL):c.1139+16_1139+21del	LPL	Deletion (intron variant)	not provided	GLikely benign
Select item 2804234	NM_000237.3(LPL):c.776-8T>C	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2798424	NM_000237.3(LPL):c.465C>G (p.Leu155=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2797167	NM_000237.3(LPL):c.429+20A>G	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 2795633	NM_000237.3(LPL):c.1158dup (p.Lys387Ter)	LPL (K387*)	Duplication (nonsense)	not provided	GPathogenic
Select item 2794861	NM_000237.3(LPL):c.1140-16T>C	LPL	Single nucleotide variant (intron 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 2781243	NM_000237.3(LPL):c.939G>C (p.Leu313=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2779585	NM_000237.3(LPL):c.902T>G (p.Leu301Arg)	LPL (L301R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2776411	NM_000237.3(LPL):c.294C>T (p.Ala98=)	LPL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2772394	NM_000237.3(LPL):c.1323-16C>T	LPL	Single nucleotide variant (intron variant)	not provided	GLikely benign

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