Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000203691 | SCV000261515 | uncertain significance | Alstrom syndrome | 2022-02-24 | criteria provided, single submitter | clinical testing | This sequence change replaces cysteine, which is neutral and slightly polar, with arginine, which is basic and polar, at codon 337 of the ALMS1 protein (p.Cys337Arg). This variant is present in population databases (rs746923506, gnomAD 0.02%). This variant has not been reported in the literature in individuals affected with ALMS1-related conditions. ClinVar contains an entry for this variant (Variation ID: 220730). In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. |
Counsyl | RCV000203691 | SCV000789088 | uncertain significance | Alstrom syndrome | 2017-01-05 | criteria provided, single submitter | clinical testing | |
Stanford Center for Inherited Cardiovascular Disease, |
RCV000786092 | SCV000924729 | uncertain significance | not provided | 2016-02-17 | no assertion criteria provided | provider interpretation | |
Natera, |
RCV000203691 | SCV002080400 | uncertain significance | Alstrom syndrome | 2021-08-19 | no assertion criteria provided | clinical testing |