Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Laboratory for Molecular Medicine, |
RCV000037308 | SCV000060965 | likely benign | not specified | 2012-06-01 | criteria provided, single submitter | clinical testing | Val158Val in exon 5 of DSG2: This variant is not expected to have clinical signi ficance because it does not alter an amino acid residue and is not located withi n the splice consensus sequence. Val158Val in exon 5 of DSG2 (allele frequency = n/a) |