Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Counsyl | RCV000409677 | SCV000485437 | likely pathogenic | Autosomal recessive limb-girdle muscular dystrophy type 2D | 2015-12-11 | criteria provided, single submitter | clinical testing | |
Revvity Omics, |
RCV000409677 | SCV002019195 | likely pathogenic | Autosomal recessive limb-girdle muscular dystrophy type 2D | 2019-01-11 | criteria provided, single submitter | clinical testing |