Whole-genome data for the root-cause workup.
Most functional-medicine workflows already include a methylation panel and a hormone panel. Mosaic adds the genomic layer underneath: every variant in every relevant gene, at 30× clinical depth, ready to share with the rest of the workup.
Free to create. Kits and every report at wholesale with a practice margin; exact pricing unlocks on approval, usually within one business day.
Three reasons it fits the work you already do.
Whole-pathway, not just MTHFR
C677T and A1298C are the variants most clients arrive asking about. Mosaic also reads MTR, MTRR, BHMT, COMT, and CBS, the rest of the methylation cycle, plus the detox and hormone-clearance pathways that interact with it. The pattern across the cycle is what shapes the protocol.
Defensible in clinical conversation
CLIA-, COLA-, CAP-, and AABB-accredited lab partner. State-permitted in NY, PA, MD and licensed in CA, RI. Variant calls reliable enough to act on, and to refer back to in a chart note without qualification.
Genomic context for the labs you already run
A DUTCH panel shows estrogen metabolites; the genome shows the COMT and CYP1A1 variants shaping how they got there. An organic-acids test flags a methylation slowdown; the genome shows whether MTHFR, MTR, or MTRR is the bottleneck. Mosaic is the layer that explains the functional panels instead of repeating them.
Used by 200+ provider practices.
200+
provider practices
5,000+
kits delivered
Every provider account includes
- Wholesale whole-genome kits at 30× depth from a CLIA-, COLA-, CAP-, and AABB-accredited lab
- The Provider Guide: gene-by-gene interpretation, watermarked to you
- Direct support from the Mosaic clinical team, usually within one business day
Ready to open your provider account?
Creating a provider account is free. Wholesale pricing and the Provider Guide unlock the moment you are approved, usually within one business day.