List of variants in gene LIPC reported as uncertain significance for hyperlipoproteinemia

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: 46

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HGVS	dbSNP	gnomAD frequency
NM_000236.3(LIPC):c.1214C>T (p.Thr405Met)	rs113298164	0.00299
NM_000236.3(LIPC):c.89-4G>A	rs184587533	0.00184
NM_000236.3(LIPC):c.588G>A (p.Ala196=)	rs34351746	0.00132
NM_000236.3(LIPC):c.866C>T (p.Ser289Phe)	rs121912502	0.00076
NM_000236.3(LIPC):c.1226A>C (p.Asp409Ala)	rs142036980	0.00071
NM_000236.3(LIPC):c.1415A>T (p.Asp472Val)	rs34596532	0.00044
NM_000236.3(LIPC):c.67C>T (p.Leu23Phe)	rs145398861	0.00034
NM_000236.3(LIPC):c.738_739dup (p.Gly247fs)	rs749932377	0.00023
NM_000236.3(LIPC):c.1430G>A (p.Arg477His)	rs148828229	0.00016
NM_000236.3(LIPC):c.317C>T (p.Ala106Val)	rs182603751	0.00013
NM_000236.3(LIPC):c.1388+13T>G	rs374479609	0.00012
NM_000236.3(LIPC):c.998G>A (p.Arg333Gln)	rs200889722	0.00011
NM_000236.3(LIPC):c.739G>A (p.Gly247Arg)	rs371573112	0.00009
NM_000236.3(LIPC):c.207G>A (p.Pro69=)	rs200127425	0.00008
NM_000236.3(LIPC):c.316G>A (p.Ala106Thr)	rs141018530	0.00007
NM_000236.3(LIPC):c.403C>T (p.Arg135Cys)	rs201014789	0.00007
NM_000236.3(LIPC):c.206C>T (p.Pro69Leu)	rs143550925	0.00006
NM_000236.3(LIPC):c.88+5G>C	rs201219858	0.00006
NM_000236.3(LIPC):c.1170G>A (p.Leu390=)	rs375751743	0.00005
NM_000236.3(LIPC):c.674G>A (p.Arg225Gln)	rs575306493	0.00005
NM_000236.3(LIPC):c.1203C>T (p.Ser401=)	rs768982423	0.00004
NM_000236.3(LIPC):c.1330C>T (p.Arg444Cys)	rs573340043	0.00004
NM_000236.3(LIPC):c.1341C>T (p.Gly447=)	rs200353965	0.00003
NM_000236.3(LIPC):c.314C>T (p.Ala105Val)	rs762938550	0.00003
NM_000236.3(LIPC):c.456+5C>T	rs529860942	0.00003
NM_000236.3(LIPC):c.1421T>C (p.Leu474Pro)	rs1442168223	0.00002
NM_000236.3(LIPC):c.132G>A (p.Thr44=)	rs755990193	0.00001
NM_000236.3(LIPC):c.1024G>A (p.Val342Ile)
NM_000236.3(LIPC):c.1031G>A (p.Arg344Gln)
NM_000236.3(LIPC):c.1052-13TC[6]	rs776858148
NM_000236.3(LIPC):c.1169+11G>A	rs762534927
NM_000236.3(LIPC):c.1215G>T (p.Thr405=)	rs755044244
NM_000236.3(LIPC):c.1231G>A (p.Gly411Ser)	rs559266901
NM_000236.3(LIPC):c.1232G>T (p.Gly411Val)	rs1894244560
NM_000236.3(LIPC):c.1273G>C (p.Val425Leu)	rs760387937
NM_000236.3(LIPC):c.353G>A (p.Gly118Glu)
NM_000236.3(LIPC):c.377C>A (p.Ala126Asp)
NM_000236.3(LIPC):c.456+2T>C	rs373200197
NM_000236.3(LIPC):c.461C>A (p.Ser154Tyr)	rs756518358
NM_000236.3(LIPC):c.575-5A>G	rs777246707
NM_000236.3(LIPC):c.787A>G (p.Ile263Val)	rs1893514095
NM_000236.3(LIPC):c.829T>C (p.Cys277Arg)	rs1224582155
NM_000236.3(LIPC):c.867C>T (p.Ser289=)	rs765258214
NM_000236.3(LIPC):c.88+8C>A
NM_000236.3(LIPC):c.947G>T (p.Cys316Phe)	rs995976417
NM_000236.3(LIPC):c.986G>A (p.Arg329His)	rs149195239

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