ClinVar Miner

Submissions for variant NM_001105206.3(LAMA4):c.1374G>A (p.Glu458=)

dbSNP: rs397516717
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000037333 SCV000060990 likely benign not specified 2012-07-24 criteria provided, single submitter clinical testing Glu451Glu in exon 12 of LAMA4: This variant is not expected to have clinical sig nificance because it does not alter an amino acid residue and is not located wit hin the splice consensus sequence. Glu451Glu in exon 12 of LAMA4 (allele freque ncy = n/a)

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