List of variants in gene LAMC3 reported as uncertain significance by Genetic Services Laboratory, University of Chicago

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: 28

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_006059.4(LAMC3):c.4160C>T (p.Ala1387Val)	rs141497885	0.00258
NM_006059.4(LAMC3):c.4130C>T (p.Thr1377Ile)	rs144662546	0.00189
NM_006059.4(LAMC3):c.1520-6G>A	rs192031352	0.00175
NM_006059.4(LAMC3):c.2066C>T (p.Pro689Leu)	rs113443891	0.00123
NM_006059.4(LAMC3):c.2276G>A (p.Gly759Asp)	rs150859618	0.00084
NM_006059.4(LAMC3):c.2227A>G (p.Asn743Asp)	rs36030184	0.00079
NM_006059.4(LAMC3):c.2987G>A (p.Arg996His)	rs113785045	0.00063
NM_006059.4(LAMC3):c.2238G>A (p.Ala746=)	rs141918703	0.00044
NM_006059.4(LAMC3):c.514G>A (p.Gly172Ser)	rs149767552	0.00039
NM_006059.4(LAMC3):c.2201A>T (p.Glu734Val)	rs376100801	0.00021
NM_006059.4(LAMC3):c.2351G>A (p.Arg784Gln)	rs371815223	0.00019
NM_006059.4(LAMC3):c.1330C>T (p.Arg444Cys)	rs140066207	0.00016
NM_006059.4(LAMC3):c.538C>T (p.Arg180Cys)	rs146609763	0.00016
NM_006059.4(LAMC3):c.1051C>T (p.Arg351Cys)	rs201626968	0.00014
NM_006059.4(LAMC3):c.2949C>T (p.Cys983=)	rs373660982	0.00008
NM_006059.4(LAMC3):c.4540C>T (p.Arg1514Cys)	rs145980204	0.00006
NM_006059.4(LAMC3):c.460G>A (p.Asp154Asn)	rs200873204	0.00005
NM_006059.4(LAMC3):c.3192G>T (p.Gln1064His)	rs373353612	0.00004
NM_006059.4(LAMC3):c.1907G>A (p.Arg636His)	rs753991024	0.00002
NM_006059.4(LAMC3):c.1978C>T (p.Arg660Trp)	rs374264939	0.00002
NM_006059.4(LAMC3):c.3019G>A (p.Gly1007Ser)	rs141105450	0.00002
NM_006059.4(LAMC3):c.1915G>A (p.Val639Ile)	rs370174192	0.00001
NM_006059.4(LAMC3):c.818G>A (p.Cys273Tyr)	rs747699617	0.00001
NM_006059.4(LAMC3):c.1865C>G (p.Pro622Arg)	rs142041428
NM_006059.4(LAMC3):c.1939G>A (p.Gly647Ser)	rs144242690
NM_006059.4(LAMC3):c.2836_2853del (p.Ala946_Gln951del)	rs2133318070
NM_006059.4(LAMC3):c.3064G>A (p.Glu1022Lys)	rs954997195
NM_006059.4(LAMC3):c.3069+8G>T	rs563444562

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.