List of variants in gene LAMC3 reported as likely benign by Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_006059.4(LAMC3):c.2516C>T (p.Thr839Met)	rs57816762	0.00893
NM_006059.4(LAMC3):c.2039C>T (p.Thr680Met)	rs73658916	0.00851
NM_006059.4(LAMC3):c.146A>G (p.Gln49Arg)	rs201962705	0.00645
NM_006059.4(LAMC3):c.2438G>A (p.Ser813Asn)	rs55741126	0.00598
NM_006059.4(LAMC3):c.1630+5C>G	rs184221540	0.00178
NM_006059.4(LAMC3):c.2439C>G (p.Ser813Arg)	rs61637370
NM_006059.4(LAMC3):c.3250G>C (p.Glu1084Gln)	rs146221263
NM_006059.4(LAMC3):c.3379G>A (p.Glu1127Lys)	rs140955110

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