ClinVar Miner

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

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Gene type:
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Total variants: 18
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HGVS dbSNP gnomAD frequency
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.*1011T>C rs115403627 0.00465
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.1262G>A (p.Gly421Glu) rs148753246 0.00185
NM_005562.3(LAMC2):c.2736T>C (p.Asn912=) rs146196115 0.00170
NM_005562.3(LAMC2):c.889A>G (p.Thr297Ala) rs143817389 0.00144
NM_005562.3(LAMC2):c.509G>T (p.Arg170Leu) rs141806165 0.00094
NM_005562.3(LAMC2):c.3206C>T (p.Thr1069Met) rs139043074 0.00072
NM_005562.3(LAMC2):c.*848C>T rs546806342 0.00023
NM_005562.3(LAMC2):c.1491T>G (p.Ala497=) rs539212332 0.00016
NM_005562.3(LAMC2):c.589C>T (p.Arg197Cys) rs184817147 0.00013
NM_005562.3(LAMC2):c.*1324C>T rs183760448
NM_005562.3(LAMC2):c.*875G>A rs10797863
NM_005562.3(LAMC2):c.2570G>C (p.Arg857Pro) rs144908769

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