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Official Description

Rare diseases (constitutional/heritable disorders), whole genome 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, proband

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Short Descr RARE DS GEN DNA ALYS PROBAND
Medium Descr RARE DS WHL GEN&MITOCHDRL DNA SEQ ALYS PROBAND
Long Descr Rare diseases (constitutional/heritable disorders), whole genome 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, proband
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
Date
Action
Notes
2021-01-01 Added First appearance in codebook.
2020-10-01 Added Code added.
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