ClinVar Miner

List of variants in gene LAMC2 reported by PreventionGenetics, part of Exact Sciences

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Total variants: 27
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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.2198G>C (p.Ser733Thr) rs2296303 0.16512
NM_005562.3(LAMC2):c.3367C>T (p.Leu1123=) rs587281 0.03867
NM_005562.3(LAMC2):c.2035C>T (p.Leu679Phe) rs62640910 0.01374
NM_005562.3(LAMC2):c.3546A>G (p.Pro1182=) rs41314547 0.00540
NM_005562.3(LAMC2):c.493C>T (p.Arg165Cys) rs142335339 0.00261
NM_005562.3(LAMC2):c.2150G>A (p.Arg717Gln) rs62640911 0.00225
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.3459G>A (p.Arg1153=) rs140649374 0.00150
NM_005562.3(LAMC2):c.884G>A (p.Arg295Gln) rs141901570 0.00132
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.2970C>A (p.Thr990=) rs182929815 0.00049
NM_005562.3(LAMC2):c.599C>A (p.Ala200Glu) rs138266625 0.00042
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.1362C>T (p.His454=) rs779680054 0.00003
NM_005562.3(LAMC2):c.80-2A>G rs771613805 0.00002
NM_005562.3(LAMC2):c.1266G>A (p.Gly422=)
NM_005562.3(LAMC2):c.146_150dup (p.Phe51fs) rs1057517353
NM_005562.3(LAMC2):c.1796G>T (p.Gly599Val)
NM_005562.3(LAMC2):c.2570G>C (p.Arg857Pro) rs144908769

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