ClinVar Miner

List of variants in gene LAMA2 reported as pathogenic by Fulgent Genetics,Fulgent Genetics

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Total variants: 4
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HGVS dbSNP
NM_000426.3(LAMA2):c.3976C>T (p.Arg1326Ter) rs398123373
NM_000426.3(LAMA2):c.5116C>T (p.Arg1706Ter) rs758775001
NM_000426.3(LAMA2):c.7074C>A (p.Tyr2358Ter) rs762806915
NM_000426.3(LAMA2):c.7732C>T (p.Arg2578Ter) rs121913572

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