ClinVar Miner

List of variants in gene LAMA2 reported by Department of Medical Genetics, National Institute of Health

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_000426.4(LAMA2):c.2164G>A (p.Glu722Lys)
NM_000426.4(LAMA2):c.2217G>A (p.Trp739Ter)	rs192317605
NM_000426.4:c.(6992+1_6993-1)_(7300+1_7301-1)del

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