ClinVar Miner

List of variants in gene LAMA2 reported as likely benign for Muscular dystrophy, limb-girdle, autosomal recessive 23

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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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000426.4(LAMA2):c.4487C>T (p.Ala1496Val)	rs147077184	0.00338
NM_000426.4(LAMA2):c.2217G>T (p.Trp739Cys)	rs192317605	0.00039

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