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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 29

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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.*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.*856C>T	rs116496189	0.00479
NM_005562.3(LAMC2):c.2422C>G (p.Pro808Ala)	rs144355456	0.00439
NM_005562.3(LAMC2):c.3000T>A (p.Ala1000=)	rs78793848	0.00161
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.*875G>T	rs10797863
NM_005562.3(LAMC2):c.1066+12C>A	rs12092752

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