Your healthcare team can provide you with more information if you are interested, or you may contact Novo Nordisk at 1-800-727-6500
The trials enrolled patients with homozygous or presumed compound heterozygous pathogenic, likely pathogenic variants, or VUS for either the POMCor PCSK1genes (Trial 3) or the LEPRgene (Trial 4)
Smeltzer, M.D
Whether you have diabetes, prediabetes, or issues with controlling your blood sugar levels, youll want to make reversing insulin resistance a top priority
If multiple formats are available, choose VCF (.vcf) or the default raw data export (.txt or .csv) If the download is a .zip or .gz file, unzip it first Upload the resulting .txt, .csv, or .vcf file above Compatible providers include: 23andMe, AncestryDNA, MyHeritage, FamilyTreeDNA, Nebula Genomics, Dante Labs, Sequencing.com, SelfDecode, and most other consumer or clinical genetic testing services that let you export your raw data