ClinVar Miner

List of variants in gene LAMC2 reported as uncertain significance for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 29
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_005562.3(LAMC2):c.493C>T (p.Arg165Cys) rs142335339 0.00261
NM_005562.3(LAMC2):c.1899G>C (p.Leu633=) rs141812464 0.00257
NM_005562.3(LAMC2):c.889A>G (p.Thr297Ala) rs143817389 0.00144
NM_005562.3(LAMC2):c.196G>A (p.Glu66Lys) rs146325169 0.00114
NM_005562.3(LAMC2):c.1318A>G (p.Ile440Val) rs147889360 0.00061
NM_005562.3(LAMC2):c.599C>A (p.Ala200Glu) rs138266625 0.00042
NM_005562.3(LAMC2):c.2014+5T>C rs377208927 0.00024
NM_005562.3(LAMC2):c.1555T>C (p.Cys519Arg) rs139464408 0.00013
NM_005562.3(LAMC2):c.2777G>A (p.Arg926His) rs201251711 0.00012
NM_005562.3(LAMC2):c.1039C>T (p.Arg347Cys) rs188149266 0.00009
NM_005562.3(LAMC2):c.2015G>C (p.Gly672Ala) rs765743445 0.00008
NM_005562.3(LAMC2):c.847T>C (p.Ser283Pro) rs763119021 0.00002
NC_000001.10:g.(?_183155488)_(183212535_?)dup
NM_005562.3(LAMC2):c.1637_1651del (p.Ala546_Cys550del) rs763146806
NM_005562.3(LAMC2):c.2012A>T (p.Glu671Val)
NM_005562.3(LAMC2):c.2420_2421delinsAT (p.Ser807Asn) rs1558097292
NM_005562.3(LAMC2):c.2423C>T (p.Pro808Leu)
NM_005562.3(LAMC2):c.2921_2923del (p.Lys974del)
NM_005562.3(LAMC2):c.2967G>C (p.Lys989Asn) rs1553267625
NM_005562.3(LAMC2):c.3086A>C (p.Asn1029Thr)
NM_005562.3(LAMC2):c.3328+1G>A rs1475860578
NM_005562.3(LAMC2):c.3328+5G>C
NM_005562.3(LAMC2):c.3415C>T (p.Arg1139Trp)
NM_005562.3(LAMC2):c.395A>G (p.Gln132Arg)
NM_005562.3(LAMC2):c.433G>A (p.Gly145Ser)
NM_005562.3(LAMC2):c.614A>G (p.His205Arg)
NM_005562.3(LAMC2):c.643G>A (p.Val215Ile)
NM_005562.3(LAMC2):c.832G>C (p.Gly278Arg)
NM_005562.3(LAMC2):c.92A>G (p.Asn31Ser)

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.