List of variants in gene LIPC studied for hyperlipoproteinemia

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 67

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HGVS	dbSNP	gnomAD frequency
NM_000236.3(LIPC):c.1068C>A (p.Phe356Leu)	rs3829462	0.94349
NM_000236.3(LIPC):c.1098A>G (p.Thr366=)	rs3829461	0.94335
NM_000236.3(LIPC):c.465G>T (p.Val155=)	rs690	0.55073
NM_000236.3(LIPC):c.644A>G (p.Asn215Ser)	rs6083	0.48324
NM_000236.3(LIPC):c.672C>G (p.Thr224=)	rs6084	0.41373
NM_000236.3(LIPC):c.591A>G (p.Gly197=)	rs6082	0.10413
NM_000236.3(LIPC):c.283G>A (p.Val95Met)	rs6078	0.05370
NM_000236.3(LIPC):c.575-8C>A	rs6080	0.02543
NM_000236.3(LIPC):c.264C>T (p.His88=)	rs7175412	0.01209
NM_000236.3(LIPC):c.837C>T (p.His279=)	rs146299102	0.00443
NM_000236.3(LIPC):c.575-15C>T	rs141216569	0.00344
NM_000236.3(LIPC):c.1214C>T (p.Thr405Met)	rs113298164	0.00299
NM_000236.3(LIPC):c.1233C>T (p.Gly411=)	rs79985029	0.00282
NM_000236.3(LIPC):c.213G>A (p.Thr71=)	rs113174258	0.00216
NM_000236.3(LIPC):c.1314A>G (p.Pro438=)	rs75983069	0.00210
NM_000236.3(LIPC):c.1052-10C>G	rs58453124	0.00202
NM_000236.3(LIPC):c.89-4G>A	rs184587533	0.00184
NM_000236.3(LIPC):c.981C>T (p.His327=)	rs142741286	0.00179
NM_000236.3(LIPC):c.588G>A (p.Ala196=)	rs34351746	0.00132
NM_000236.3(LIPC):c.1064A>G (p.Gln355Arg)	rs140272400	0.00112
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.1029G>A (p.Thr343=)	rs570824458	0.00008
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.1068= (p.Phe356=)
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.1437C>A (p.Thr479=)	rs6074
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.583G>A (p.Ala195Thr)	rs1566946168
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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