ClinVar Miner

List of variants in gene LAMC2 reported by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 136
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_005562.3(LAMC2):c.268+14A>G rs647347 0.45636
NM_005562.3(LAMC2):c.798T>G (p.Gly266=) rs1047980 0.29549
NM_005562.3(LAMC2):c.2688G>A (p.Gln896=) rs1047981 0.29455
NM_005562.3(LAMC2):c.483C>T (p.Val161=) rs1129723 0.25575
NM_005562.3(LAMC2):c.297C>T (p.Ser99=) rs2274980 0.25565
NM_005562.3(LAMC2):c.*13T>G rs3768593 0.23969
NM_005562.3(LAMC2):c.2198G>C (p.Ser733Thr) rs2296303 0.16512
NM_005562.3(LAMC2):c.371C>T (p.Thr124Met) rs11586699 0.05840
NM_005562.3(LAMC2):c.*746G>T rs587387 0.04604
NM_005562.3(LAMC2):c.*928A>G rs553836 0.04025
NM_005562.3(LAMC2):c.*310G>A rs599630 0.04005
NM_005562.3(LAMC2):c.3367C>T (p.Leu1123=) rs587281 0.03867
NM_005562.3(LAMC2):c.331G>C (p.Ala111Pro) rs12065473 0.03585
NM_005562.3(LAMC2):c.741C>A (p.Asp247Glu) rs2296306 0.03381
NM_005562.3(LAMC2):c.*362T>C rs6687880 0.03325
NM_005562.3(LAMC2):c.*600A>G rs77018464 0.01559
NM_005562.3(LAMC2):c.2035C>T (p.Leu679Phe) rs62640910 0.01374
NM_005562.3(LAMC2):c.344G>A (p.Arg115Gln) rs17481405 0.00892
NM_005562.3(LAMC2):c.269-15C>T rs12085883 0.00715
NM_005562.3(LAMC2):c.*133C>A rs114841922 0.00698
NM_005562.3(LAMC2):c.*749G>A rs146315432 0.00613
NM_005562.3(LAMC2):c.*1235G>C rs74129665 0.00542
NM_005562.3(LAMC2):c.3546A>G (p.Pro1182=) rs41314547 0.00540
NM_005562.3(LAMC2):c.*999C>G rs73055716 0.00490
NM_005562.3(LAMC2):c.*856C>T rs116496189 0.00479
NM_005562.3(LAMC2):c.*1011T>C rs115403627 0.00465
NM_005562.3(LAMC2):c.*275A>C rs183342651 0.00455
NM_005562.3(LAMC2):c.2422C>G (p.Pro808Ala) rs144355456 0.00439
NM_005562.3(LAMC2):c.2754+9T>C rs113467864 0.00434
NM_005562.3(LAMC2):c.880C>T (p.Leu294=) rs144572936 0.00307
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.*1398C>T rs564740740 0.00237
NM_005562.3(LAMC2):c.1262G>A (p.Gly421Glu) rs148753246 0.00185
NM_005562.3(LAMC2):c.1637C>A (p.Ala546Asp) rs140949383 0.00177
NM_005562.3(LAMC2):c.*405C>T rs148313302 0.00173
NM_005562.3(LAMC2):c.2736T>C (p.Asn912=) rs146196115 0.00170
NM_005562.3(LAMC2):c.3000T>A (p.Ala1000=) rs78793848 0.00161
NM_005562.3(LAMC2):c.3459G>A (p.Arg1153=) rs140649374 0.00150
NM_005562.3(LAMC2):c.889A>G (p.Thr297Ala) rs143817389 0.00144
NM_005562.3(LAMC2):c.884G>A (p.Arg295Gln) rs141901570 0.00132
NM_005562.3(LAMC2):c.407A>T (p.Asp136Val) rs12037099 0.00130
NM_005562.3(LAMC2):c.*1097C>T rs76939882 0.00128
NM_005562.3(LAMC2):c.80-6C>T rs78056473 0.00117
NM_005562.3(LAMC2):c.*200G>A rs114356159 0.00114
NM_005562.3(LAMC2):c.196G>A (p.Glu66Lys) rs146325169 0.00114
NM_005562.3(LAMC2):c.2387C>T (p.Ala796Val) rs139718245 0.00106
NM_005562.3(LAMC2):c.509G>T (p.Arg170Leu) rs141806165 0.00094
NM_005562.3(LAMC2):c.*1617A>G rs532073148 0.00088
NM_005562.3(LAMC2):c.2681G>A (p.Arg894His) rs146907099 0.00081
NM_005562.3(LAMC2):c.3354G>A (p.Glu1118=) rs149718832 0.00081
NM_005562.3(LAMC2):c.*1686G>A rs540729716 0.00078
NM_005562.3(LAMC2):c.2634G>A (p.Ala878=) rs148925665 0.00076
NM_005562.3(LAMC2):c.2892C>T (p.Asn964=) rs147657304 0.00073
NM_005562.3(LAMC2):c.3206C>T (p.Thr1069Met) rs139043074 0.00072
NM_005562.3(LAMC2):c.1318A>G (p.Ile440Val) rs147889360 0.00061
NM_005562.3(LAMC2):c.*1053C>T rs575918658 0.00053
NM_005562.3(LAMC2):c.599C>A (p.Ala200Glu) rs138266625 0.00042
NM_005562.3(LAMC2):c.*630C>G rs141968850 0.00041
NM_005562.3(LAMC2):c.*848C>T rs546806342 0.00023
NM_005562.3(LAMC2):c.1147A>G (p.Ile383Val) rs199729402 0.00021
NM_005562.3(LAMC2):c.*1008C>T rs886045635 0.00016
NM_005562.3(LAMC2):c.1422G>A (p.Pro474=) rs148065050 0.00016
NM_005562.3(LAMC2):c.1491T>G (p.Ala497=) rs539212332 0.00016
NM_005562.3(LAMC2):c.503+6T>C rs375623003 0.00016
NM_005562.3(LAMC2):c.954-15T>C rs370813334 0.00014
NM_005562.3(LAMC2):c.1555T>C (p.Cys519Arg) rs139464408 0.00013
NM_005562.3(LAMC2):c.589C>T (p.Arg197Cys) rs184817147 0.00013
NM_005562.3(LAMC2):c.2014+12C>A rs370051807 0.00012
NM_005562.3(LAMC2):c.2777G>A (p.Arg926His) rs201251711 0.00012
NM_005562.3(LAMC2):c.*1482A>G rs377075989 0.00011
NM_005562.3(LAMC2):c.3246G>A (p.Gln1082=) rs138728557 0.00011
NM_005562.3(LAMC2):c.795T>C (p.Tyr265=) rs201246173 0.00011
NM_005562.3(LAMC2):c.*297C>A rs886045631 0.00010
NM_005562.3(LAMC2):c.1074G>A (p.Gly358=) rs145811533 0.00009
NM_005562.3(LAMC2):c.*1031A>G rs1179352123 0.00008
NM_005562.3(LAMC2):c.590G>A (p.Arg197His) rs376553923 0.00007
NM_005562.3(LAMC2):c.*986T>A rs536483830 0.00006
NM_005562.3(LAMC2):c.3273T>G (p.Ala1091=) rs201445121 0.00006
NM_005562.3(LAMC2):c.1036C>G (p.Leu346Val) rs754799907 0.00005
NM_005562.3(LAMC2):c.503+14G>A rs372097432 0.00005
NM_005562.3(LAMC2):c.*1637G>A rs886045643 0.00004
NM_005562.3(LAMC2):c.1597C>T (p.Arg533Trp) rs1029109781 0.00004
NM_005562.3(LAMC2):c.3033C>T (p.Ala1011=) rs771520608 0.00004
NM_005562.3(LAMC2):c.*1021C>T rs987683532 0.00003
NM_005562.3(LAMC2):c.*816A>T rs886045634 0.00003
NM_005562.3(LAMC2):c.1215G>A (p.Ala405=) rs774558289 0.00003
NM_005562.3(LAMC2):c.2081G>A (p.Arg694His) rs142509506 0.00003
NM_005562.3(LAMC2):c.3448C>T (p.Arg1150Cys) rs779406247 0.00003
NM_005562.3(LAMC2):c.*1674T>A rs886045645 0.00002
NM_005562.3(LAMC2):c.*846T>C rs1482045103 0.00002
NM_005562.3(LAMC2):c.*976C>A rs937726448 0.00002
NM_005562.3(LAMC2):c.1066A>G (p.Ser356Gly) rs747095585 0.00002
NM_005562.3(LAMC2):c.1268C>A (p.Ala423Asp) rs886045626 0.00002
NM_005562.3(LAMC2):c.1675G>A (p.Gly559Arg) rs555090268 0.00002
NM_005562.3(LAMC2):c.2555T>C (p.Leu852Pro) rs376232873 0.00002
NM_005562.3(LAMC2):c.733C>T (p.Arg245Ter) rs118203901 0.00002
NM_005562.3(LAMC2):c.*1059G>A rs886045637 0.00001
NM_005562.3(LAMC2):c.*1456T>C rs886045642 0.00001
NM_005562.3(LAMC2):c.*1647A>G rs886045644 0.00001
NM_005562.3(LAMC2):c.*1700G>A rs1159161006 0.00001
NM_005562.3(LAMC2):c.2221-1G>A rs1558096586 0.00001
NM_005562.3(LAMC2):c.2418T>A (p.Gly806=) rs553672320 0.00001
NM_005562.3(LAMC2):c.2456+15G>A rs532836837 0.00001
NM_005562.3(LAMC2):c.2545C>T (p.Leu849Phe) rs1244239473 0.00001
NM_005562.3(LAMC2):c.3449G>A (p.Arg1150His) rs748464019 0.00001
NM_005562.3(LAMC2):c.461G>A (p.Arg154His) rs774844905 0.00001
NM_005562.3(LAMC2):c.80T>C (p.Val27Ala) rs772538256 0.00001
NM_005562.3(LAMC2):c.*1033AT[2] rs886045636
NM_005562.3(LAMC2):c.*1066G>C rs886045638
NM_005562.3(LAMC2):c.*1067C>T rs886045639
NM_005562.3(LAMC2):c.*1138T>C rs1313225593
NM_005562.3(LAMC2):c.*1139A>T rs192080195
NM_005562.3(LAMC2):c.*1199G>A rs886045640
NM_005562.3(LAMC2):c.*1244C>G rs542862063
NM_005562.3(LAMC2):c.*1265G>C rs886045641
NM_005562.3(LAMC2):c.*1324C>T rs183760448
NM_005562.3(LAMC2):c.*1650A>G rs919395948
NM_005562.3(LAMC2):c.*400T>C rs886045632
NM_005562.3(LAMC2):c.*593A>G rs886045633
NM_005562.3(LAMC2):c.*875G>A rs10797863
NM_005562.3(LAMC2):c.*875G>T rs10797863
NM_005562.3(LAMC2):c.1032A>C (p.Thr344=) rs1659605215
NM_005562.3(LAMC2):c.1066+12C>A rs12092752
NM_005562.3(LAMC2):c.1259G>C (p.Gly420Ala) rs763994158
NM_005562.3(LAMC2):c.1286-4C>T rs944567230
NM_005562.3(LAMC2):c.2529G>C (p.Arg843Ser) rs762064570
NM_005562.3(LAMC2):c.2570G>C (p.Arg857Pro) rs144908769
NM_005562.3(LAMC2):c.2658C>G (p.Thr886=) rs1659999214
NM_005562.3(LAMC2):c.2994G>C (p.Gly998=) rs1660064320
NM_005562.3(LAMC2):c.3158T>A (p.Met1053Lys) rs570770124
NM_005562.3(LAMC2):c.3166G>A (p.Val1056Met) rs886045627
NM_005562.3(LAMC2):c.3346G>T (p.Asp1116Tyr) rs886045628
NM_005562.3(LAMC2):c.3411A>G (p.Gln1137=) rs886045629
NM_005562.3(LAMC2):c.3503C>A (p.Ala1168Asp) rs886045630
NM_005562.3(LAMC2):c.739G>C (p.Asp247His) rs773715293

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.