ClinVar Miner

Submissions for variant NM_000426.4(LAMA2):c.4860+2delinsGGCC

dbSNP: rs1562497781
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000709618 SCV000839534 pathogenic Muscular dystrophy, limb-girdle, autosomal recessive 23 2018-10-05 no assertion criteria provided literature only

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