Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Laboratory for Molecular 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) |