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

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: 10

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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.2150G>A (p.Arg717Gln)	rs62640911	0.00225

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