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| Short Descr | RARE DS WHL GEN SEQ FTL SAMP | Medium Descr | RARE DS WHL GENOM SEQ ALYS CHRMOML ABNR FTL SAMP | Long Descr | Rare diseases (constitutional/heritable disorders), whole genome sequence analysis for chromosomal abnormalities, copy number variants, duplications/deletions, inversions, unbalanced translocations, regions of homozygosity (ROH), inheritance pattern that indicate uniparental disomy (UPD), and aneuploidy, fetal sample (amniotic fluid, chorionic villus sample, or products of conception), identification and categorization of genetic variants, diagnostic report of fetal results based on phenotype with maternal sample and paternal sample, if performed, as comparators and/or maternal cell contamination | CLIA Waived (QW) | No | APC Status Indicator | Service Paid under Fee Schedule or Payment System other than OPPS | Berenson-Eggers TOS (BETOS) | none | MUE | 2 |
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| 2025-01-01 | Added | First appearance in codebook. |
| 2024-07-01 | Added | Code added. |
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