Total submissions: 6
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Eurofins Ntd Llc |
RCV000175715 | SCV000227251 | benign | not specified | 2015-03-06 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001721108 | SCV000531153 | likely benign | not provided | 2019-04-02 | criteria provided, single submitter | clinical testing | |
Labcorp Genetics |
RCV000642648 | SCV000764335 | benign | Autosomal recessive distal spinal muscular atrophy 1; Charcot-Marie-Tooth disease axonal type 2S | 2024-01-25 | criteria provided, single submitter | clinical testing | |
Molecular Genetics Laboratory, |
RCV001174182 | SCV001337308 | likely benign | Charcot-Marie-Tooth disease | criteria provided, single submitter | clinical testing | ||
Ce |
RCV001721108 | SCV003916747 | likely benign | not provided | 2023-03-01 | criteria provided, single submitter | clinical testing | IGHMBP2: BP4, BP7 |
Breakthrough Genomics, |
RCV001721108 | SCV005219388 | likely benign | not provided | criteria provided, single submitter | not provided |