ClinVar Miner

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

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Total variants: 20
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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.1262G>A (p.Gly421Glu) rs148753246 0.00185
NM_005562.3(LAMC2):c.1637C>A (p.Ala546Asp) rs140949383 0.00177
NM_005562.3(LAMC2):c.2736T>C (p.Asn912=) rs146196115 0.00170
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.2387C>T (p.Ala796Val) rs139718245 0.00108
NM_005562.3(LAMC2):c.509G>T (p.Arg170Leu) rs141806165 0.00094
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.1796G>T (p.Gly599Val) rs146687665 0.00063
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 0.00021
NM_005562.3(LAMC2):c.503+6T>C rs375623003 0.00015
NM_005562.3(LAMC2):c.1362C>T (p.His454=) rs779680054 0.00002
NM_005562.3(LAMC2):c.1266G>A (p.Gly422=) rs2526061124
NM_005562.3(LAMC2):c.2570G>C (p.Arg857Pro) rs144908769

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