ClinVar Miner

List of variants in gene LAMC2 reported by Neuberg Centre For Genomic Medicine, NCGM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_005562.3(LAMC2):c.1904C>G (p.Ser635Ter)	rs2526088461
NM_005562.3(LAMC2):c.195C>A (p.Cys65Ter)	rs2525976672
NM_005562.3(LAMC2):c.3438A>C (p.Glu1146Asp)	rs2526147589

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