List of variants in gene LPL reported as likely benign by Ambry Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 98

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HGVS	dbSNP	gnomAD frequency
NM_000237.3(LPL):c.456T>C (p.Asn152=)	rs116678290	0.00183
NM_000237.3(LPL):c.1128C>T (p.Ile376=)	rs299	0.00140
NM_000237.3(LPL):c.1136C>T (p.Thr379Ile)	rs76708715	0.00133
NM_000237.3(LPL):c.345A>C (p.Ser115=)	rs147309575	0.00088
NM_000237.3(LPL):c.786G>A (p.Gln262=)	rs140986245	0.00066
NM_000237.3(LPL):c.798C>T (p.Cys266=)	rs118204082	0.00034
NM_000237.3(LPL):c.687T>C (p.His229=)	rs45607438	0.00022
NM_000237.3(LPL):c.189C>T (p.Ser63=)	rs114726797	0.00021
NM_000237.3(LPL):c.1325T>G (p.Val442Gly)	rs116403115	0.00016
NM_000237.3(LPL):c.528C>G (p.Val176=)	rs199606532	0.00013
NM_000237.3(LPL):c.1062T>C (p.Ser354=)	rs913717970	0.00011
NM_000237.3(LPL):c.105C>T (p.Ile35=)	rs145405273	0.00010
NM_000237.3(LPL):c.525A>G (p.Lys175=)	rs757038496	0.00007
NM_000237.3(LPL):c.621C>T (p.Asp207=)	rs118204076	0.00007
NM_000237.3(LPL):c.111C>T (p.Ile37=)	rs374067507	0.00006
NM_000237.3(LPL):c.585G>A (p.Pro195=)	rs563135472	0.00005
NM_000237.3(LPL):c.804C>T (p.His268=)	rs776585907	0.00005
NM_000237.3(LPL):c.1278C>T (p.Phe426=)	rs771051928	0.00004
NM_000237.3(LPL):c.1338T>C (p.Ser446=)	rs146509813	0.00004
NM_000237.3(LPL):c.1368A>C (p.Gly456=)	rs151194635	0.00004
NM_000237.3(LPL):c.699C>T (p.Tyr233=)	rs370261979	0.00004
NM_000237.3(LPL):c.1113C>T (p.Ala371=)	rs750345655	0.00003
NM_000237.3(LPL):c.60C>T (p.Ala20=)	rs1215798253	0.00003
NM_000237.3(LPL):c.474C>T (p.Tyr158=)	rs767027334	0.00002
NM_000237.3(LPL):c.750C>T (p.Arg250=)	rs373989588	0.00002
NM_000237.3(LPL):c.1074C>T (p.Thr358=)	rs773686669	0.00001
NM_000237.3(LPL):c.1098G>A (p.Leu366=)	rs921146158	0.00001
NM_000237.3(LPL):c.1107C>T (p.Thr369=)	rs200121996	0.00001
NM_000237.3(LPL):c.1137T>A (p.Thr379=)	rs773918283	0.00001
NM_000237.3(LPL):c.1213T>C (p.Leu405=)	rs1362456283	0.00001
NM_000237.3(LPL):c.1257C>T (p.Asp419=)	rs780861348	0.00001
NM_000237.3(LPL):c.1272C>T (p.Pro424=)	rs200852756	0.00001
NM_000237.3(LPL):c.1344G>A (p.Glu448=)	rs143110734	0.00001
NM_000237.3(LPL):c.1380G>A (p.Ala460=)	rs768747119	0.00001
NM_000237.3(LPL):c.1383A>G (p.Val461=)	rs1356232479	0.00001
NM_000237.3(LPL):c.1389G>C (p.Val463=)	rs137934933	0.00001
NM_000237.3(LPL):c.462T>C (p.His154=)	rs770491860	0.00001
NM_000237.3(LPL):c.555T>C (p.Ala185=)	rs756368813	0.00001
NM_000237.3(LPL):c.618A>G (p.Val206=)	rs200700551	0.00001
NM_000237.3(LPL):c.807G>A (p.Glu269=)	rs1209674126	0.00001
NM_000237.3(LPL):c.81C>A (p.Ala27=)	rs764871141	0.00001
NM_000237.3(LPL):c.843T>C (p.Asn281=)	rs1217848191	0.00001
NM_000237.3(LPL):c.891T>C (p.Phe297=)	rs150120283	0.00001
NM_000237.3(LPL):c.900G>A (p.Gly300=)	rs748234170	0.00001
NM_000237.3(LPL):c.948G>A (p.Glu316=)	rs1352068321	0.00001
NM_000237.3(LPL):c.1005G>A (p.Gln335=)
NM_000237.3(LPL):c.1011C>T (p.Pro337=)
NM_000237.3(LPL):c.1044T>C (p.His348=)
NM_000237.3(LPL):c.1080G>A (p.Gln360=)	rs1043502015
NM_000237.3(LPL):c.1108G>A (p.Val370Met)
NM_000237.3(LPL):c.1195A>G (p.Ile399Val)
NM_000237.3(LPL):c.1275C>G (p.Gly425=)
NM_000237.3(LPL):c.135C>T (p.Thr45=)
NM_000237.3(LPL):c.1375C>T (p.Pro459Ser)
NM_000237.3(LPL):c.153G>A (p.Glu51=)
NM_000237.3(LPL):c.162C>T (p.Cys54=)	rs2128837009
NM_000237.3(LPL):c.192G>C (p.Val64=)
NM_000237.3(LPL):c.213C>T (p.His71=)	rs11542065
NM_000237.3(LPL):c.21C>A (p.Leu7=)
NM_000237.3(LPL):c.264T>C (p.Tyr88=)	rs118204065
NM_000237.3(LPL):c.276G>A (p.Val92=)	rs551959021
NM_000237.3(LPL):c.285T>G (p.Leu95=)
NM_000237.3(LPL):c.300C>T (p.Tyr100=)
NM_000237.3(LPL):c.309A>G (p.Glu103=)
NM_000237.3(LPL):c.318C>T (p.Ser106=)	rs1230163149
NM_000237.3(LPL):c.31C>T (p.Leu11=)
NM_000237.3(LPL):c.333G>T (p.Val111=)	rs749390229
NM_000237.3(LPL):c.33G>A (p.Leu11=)
NM_000237.3(LPL):c.342G>A (p.Leu114=)
NM_000237.3(LPL):c.363C>T (p.Tyr121=)
NM_000237.3(LPL):c.372C>T (p.Ser124=)	rs762600466
NM_000237.3(LPL):c.375G>A (p.Ala125=)
NM_000237.3(LPL):c.396A>T (p.Gly132=)
NM_000237.3(LPL):c.410G>A (p.Arg137Gln)
NM_000237.3(LPL):c.417C>T (p.Ile139=)	rs1453664641
NM_000237.3(LPL):c.465C>T (p.Leu155=)
NM_000237.3(LPL):c.468G>A (p.Leu156=)
NM_000237.3(LPL):c.489T>C (p.His163=)	rs2128837992
NM_000237.3(LPL):c.495T>C (p.Ala165=)	rs2128837993
NM_000237.3(LPL):c.540T>C (p.Thr180=)
NM_000237.3(LPL):c.564C>T (p.Asn188=)
NM_000237.3(LPL):c.633A>G (p.Thr211=)	rs1563575079
NM_000237.3(LPL):c.678A>G (p.Pro226=)	rs558390128
NM_000237.3(LPL):c.702G>A (p.Pro234=)	rs1474778814
NM_000237.3(LPL):c.729T>C (p.Cys243=)
NM_000237.3(LPL):c.783C>T (p.Asp261=)	rs138065727
NM_000237.3(LPL):c.789A>G (p.Leu263=)
NM_000237.3(LPL):c.795G>A (p.Lys265=)	rs1276587631
NM_000237.3(LPL):c.828C>T (p.Ile276=)	rs766760812
NM_000237.3(LPL):c.834T>A (p.Ser278=)
NM_000237.3(LPL):c.84C>G (p.Ala28=)	rs1387718651
NM_000237.3(LPL):c.888C>T (p.Ala296=)	rs2128838524
NM_000237.3(LPL):c.89A>G (p.Gln30Arg)
NM_000237.3(LPL):c.915T>C (p.Cys305=)
NM_000237.3(LPL):c.924C>T (p.Asn308=)
NM_000237.3(LPL):c.939G>A (p.Leu313=)
NM_000237.3(LPL):c.939G>C (p.Leu313=)
NM_000237.3(LPL):c.981A>G (p.Lys327=)

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