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| Short Descr | RARE DS XOM DNA ALYS EA COMP | Medium Descr | RARE DS WHL XOM&MITOCHDRL DNA SEQ ALYS EA CMPRTR | Long Descr | Rare diseases (constitutional/heritable disorders), whole exome and mitochondrial DNA sequence analysis, including small sequence changes, deletions, duplications, short tandem repeat gene expansions, and variants in non-uniquely mappable regions, blood or saliva, identification and categorization of genetic variants, each comparator exome (eg, parent, sibling) | CLIA Waived (QW) | No | APC Status Indicator | Service Paid under Fee Schedule or Payment System other than OPPS | Berenson-Eggers TOS (BETOS) | none | MUE | 1 |
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| 2021-01-01 | Added | First appearance in codebook. |
| 2020-10-01 | Added | Code added. |
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