Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Eurofins Ntd Llc |
RCV000175608 | SCV000227126 | pathogenic | not provided | 2013-01-21 | criteria provided, single submitter | clinical testing | |
Labcorp Genetics |
RCV001232128 | SCV001404674 | pathogenic | LAMA2-related muscular dystrophy | 2023-10-08 | criteria provided, single submitter | clinical testing | This sequence change creates a premature translational stop signal (p.Gly62*) in the LAMA2 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in LAMA2 are known to be pathogenic (PMID: 18700894, 32904964). This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with LAMA2-related conditions. ClinVar contains an entry for this variant (Variation ID: 92942). For these reasons, this variant has been classified as Pathogenic. |
Revvity Omics, |
RCV000175608 | SCV002022633 | likely pathogenic | not provided | 2021-08-31 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002498383 | SCV002810319 | likely pathogenic | Merosin deficient congenital muscular dystrophy; Muscular dystrophy, limb-girdle, autosomal recessive 23 | 2022-03-31 | criteria provided, single submitter | clinical testing |