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Whole Genome Sequencing For Rare Inherited Disease

Delaware rates for HCPCS 0212U

Searches for the genetic cause of a suspected rare inherited disorder in the affected patient. The person's entire genome is sequenced, together with mitochondrial DNA, and anything found is classified by how likely it is to be causing disease. Blood or saliva can be used.

Rates data updated July 2026.

How much rates vary

Facilitymedian $6,310 · 10th to 90th $6,310 to $6,310Professionalmedian $2,884 · 10th to 90th $2,884 to $4,571
$5K$10Kfacility $6,310professional $2,884

Distribution of negotiated rates across all payers (price axis is log-scale). Each curve is scaled to its own total: facility and professional rates are different services, shown together to compare where they cluster. Small sample; interpret with caution. Need provider-level prices or 24+ months of history? Contact us.

Rates by insurance carrier

Insurance Carrier
Aetna
Setting
Facility
Modifier
Global
Typical Low
$6,309.57
Median
$6,309.57
Typical High
$6,309.57
Aetna
Setting
Professional
Modifier
Global
Typical Low
$2,884.03
Median
$2,884.03
Typical High
$4,570.88
United
Setting
Professional
Modifier
Global
Typical Low
$2,290.87
Median
$3,311.31
Typical High
$8,128.31