Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Institute of Human Genetics, |
RCV001253229 | SCV001428846 | likely pathogenic | Achondrogenesis, type IB | 2018-09-24 | criteria provided, single submitter | clinical testing | This variant was identified as homozygous |
Baylor Genetics | RCV001253229 | SCV004201794 | likely pathogenic | Achondrogenesis, type IB | 2024-01-09 | criteria provided, single submitter | clinical testing | |
Labcorp Genetics |
RCV003770313 | SCV004578788 | pathogenic | Achondrogenesis, type IB; Atelosteogenesis type II; Multiple epiphyseal dysplasia type 4; Diastrophic dysplasia | 2023-07-27 | criteria provided, single submitter | clinical testing | This sequence change creates a premature translational stop signal (p.Gln79*) in the SLC26A2 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in SLC26A2 are known to be pathogenic (PMID: 7923357, 10482955, 11241838). This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with SLC26A2-related conditions. ClinVar contains an entry for this variant (Variation ID: 976051). For these reasons, this variant has been classified as Pathogenic. |