List of variants in gene LAMC3 reported as benign by CeGaT Center for Human Genetics Tuebingen

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_006059.4(LAMC3):c.3371C>T (p.Ser1124Phe)	rs113259170	0.00738
NM_006059.4(LAMC3):c.146A>G (p.Gln49Arg)	rs201962705	0.00645
NM_006059.4(LAMC3):c.558C>T (p.Arg186=)	rs2275135	0.00105

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