List of variants in gene LAMC3 reported as benign for not specified

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: 47

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_006059.4(LAMC3):c.3244A>G (p.Ser1082Gly)	rs2275140	0.75621
NM_006059.4(LAMC3):c.219T>G (p.His73Gln)	rs3739512	0.56936
NM_006059.4(LAMC3):c.1932C>T (p.Ser644=)	rs12349966	0.48282
NM_006059.4(LAMC3):c.963C>T (p.Ala321=)	rs2275131	0.40359
NM_006059.4(LAMC3):c.4378-4A>G	rs4740413	0.38051
NM_006059.4(LAMC3):c.3114C>G (p.Leu1038=)	rs10901345	0.33677
NM_006059.4(LAMC3):c.3108G>A (p.Gly1036=)	rs10901344	0.33663
NM_006059.4(LAMC3):c.521C>A (p.Pro174His)	rs2275137	0.29468
NM_006059.4(LAMC3):c.4298C>T (p.Thr1433Met)	rs7024108	0.28739
NM_006059.4(LAMC3):c.1564C>T (p.Pro522Ser)	rs869457	0.28273
NM_006059.4(LAMC3):c.4231-10C>T	rs4740411	0.20977
NM_006059.4(LAMC3):c.4376G>A (p.Arg1459Gln)	rs4740412	0.20674
NM_006059.4(LAMC3):c.1218G>A (p.Thr406=)	rs2293518	0.20549
NM_006059.4(LAMC3):c.4477+13T>C	rs2275143	0.16247
NM_006059.4(LAMC3):c.75C>T (p.Cys25=)	rs13286358	0.10217
NM_006059.3(LAMC3):c.-42C>G	rs112101828	0.06200
NM_006059.4(LAMC3):c.3790C>T (p.Arg1264Trp)	rs11244275	0.04427
NM_006059.4(LAMC3):c.92G>T (p.Arg31Leu)	rs116259120	0.02047
NM_006059.4(LAMC3):c.1939+11A>G	rs73550474	0.01979
NM_006059.4(LAMC3):c.2559C>T (p.Ser853=)	rs34652877	0.01902
NM_006059.4(LAMC3):c.-2C>T	rs137883250	0.01424
NM_006059.4(LAMC3):c.4561T>G (p.Ser1521Ala)	rs117361076	0.01275
NM_006059.4(LAMC3):c.454C>T (p.Arg152Cys)	rs45628035	0.00975
NM_006059.4(LAMC3):c.2096G>A (p.Gly699Asp)	rs61737720	0.00943
NM_006059.4(LAMC3):c.2516C>T (p.Thr839Met)	rs57816762	0.00893
NM_006059.4(LAMC3):c.2039C>T (p.Thr680Met)	rs73658916	0.00851
NM_006059.4(LAMC3):c.374-16G>A	rs145283886	0.00742
NM_006059.4(LAMC3):c.2352G>A (p.Arg784=)	rs35654564	0.00652
NM_006059.4(LAMC3):c.146A>G (p.Gln49Arg)	rs201962705	0.00645
NM_006059.4(LAMC3):c.786G>A (p.Val262=)	rs2275133	0.00543
NM_006059.4(LAMC3):c.2890+15T>A	rs115549520	0.00535
NM_006059.4(LAMC3):c.977-11C>G	rs112213059	0.00527
NM_006059.4(LAMC3):c.2891-8C>T	rs199535979	0.00339
NM_006059.4(LAMC3):c.2517G>A (p.Thr839=)	rs140540789	0.00292
NM_006059.4(LAMC3):c.3927+8C>G	rs148008251	0.00228
NM_006059.4(LAMC3):c.3347C>G (p.Ala1116Gly)	rs36028197	0.00226
NM_006059.4(LAMC3):c.1630+5C>G	rs184221540	0.00178
NM_006059.4(LAMC3):c.4653C>T (p.Ala1551=)	rs182704192	0.00057
NM_006059.4(LAMC3):c.4068G>A (p.Ala1356=)	rs377618961	0.00008
NM_006059.4(LAMC3):c.3624G>A (p.Glu1208=)	rs569440839	0.00002
NM_006059.4(LAMC3):c.2308C>G (p.Arg770Gly)	rs3739510
NM_006059.4(LAMC3):c.2438_2439delinsAG (p.Ser813Lys)	rs386738959
NM_006059.4(LAMC3):c.3070-18dup	rs34910694
NM_006059.4(LAMC3):c.3250G>C (p.Glu1084Gln)	rs146221263
NM_006059.4(LAMC3):c.4146G>C (p.Arg1382Ser)	rs147092908
NM_006059.4(LAMC3):c.521_522delinsAG (p.Pro174Gln)	rs386738954
NM_006059.4(LAMC3):c.855A>G (p.Ala285=)	rs2275132

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.