0567U* prior authorization | Cigna
0567U*, Rare diseases (constitutional/heritable disorders), whole-genome sequence analysis combination of short and long reads, for single- nucleotide variants, insertions/deletions and characterized intronic variants, copy-number variants, duplications/deletions, mobile element insertions, runs of homozygosity, aneuploidy, and inversions, mitochondrial DNA sequence and deletions, short tandem repeat genes, methylation status of selected regions, blood, saliva, amniocentesis, chorionic villus sample or tissue, identification and categorization of genetic variants, is on the Cigna prior authorization list. Not a coverage or referral decision.
- Code
- 0567U*
- Description
- Rare diseases (constitutional/heritable disorders), whole-genome sequence analysis combination of short and long reads, for single- nucleotide variants, insertions/deletions and characterized intronic variants, copy-number variants, duplications/deletions, mobile element insertions, runs of homozygosity, aneuploidy, and inversions, mitochondrial DNA sequence and deletions, short tandem repeat genes, methylation status of selected regions, blood, saliva, amniocentesis, chorionic villus sample or tissue, identification and categorization of genetic variants
- Source
- Master Precertification List For Health Care Providers, Pg 9 Original policy