The Best DNA Tests and Whole Genome Sequencing
Strongest Privacy Highest Quality Most Informative
BLACK FRIDAY SITEWIDE SUPERSALE
Ultimate DNA Test
Health + Ancestry + More
Black Friday Package
- Wellness & Longevity
- Ancestry & Geneology
- Coronavirus DNA Health Report - Comprehensive Version
- 2 Months Silver Membership
(Includes choice of any 4 additional DNA Reports) - Privacy First Data Confidentiality
Black Friday Shipping Discount: Shipping is FREE for orders shipped to the USA and 50% off for all other countries.
Obtains data on around 30 million genetic variants. For comparison, tests from 23andMe, Ancestry and MyHeritage provide data on less than 1 million genetic variants. Also includes the ability to download your raw DNA data file for no additional fee.
Obtains data on around 30 million genetic variants. For comparison, tests from 23andMe, Ancestry and MyHeritage provide data on less than 1 million genetic variants. Also includes the ability to download your raw DNA data file for no additional fee.
Ultimate Genome Sequencing
100% of your genome
(Clinical-grade whole genome sequencing)
Black Friday Package
- Wellness & Longevity
- Healthcare Pro Report
- Rare Disease Screen
- Medication & Drug Reactions
- Genetic Ancestry with Haplogroups
- Coronavirus DNA Health Report - Comprehensive Version
- 2 Months Gold Membership
(Includes choice of any 8 additional DNA Reports) - Privacy First Data Confidentiality
Black Friday Shipping Discount: Shipping is FREE for orders shipped to the USA and 50% off for all other countries.
Obtains data on around 3 billion positions within your genome (100% of your genome). Also includes the ability to download your raw genome data files for no additional fee. This includes FASTQ, BAM and VCFs covering all genetic variations: Single Nucleotide Polymorphisms (SNPs), Insertions and Deletions (INDELs), Structural Variations (SVs), Copy Number Variations (CNVs) and Mitochondrial Heteroplasmy (MITO).
Obtains data on around 3 billion positions within your genome (100% of your genome). Also includes the ability to download your raw genome data files for no additional fee. This includes FASTQ, BAM and VCFs covering all genetic variations: Single Nucleotide Polymorphisms (SNPs), Insertions and Deletions (INDELs), Structural Variations (SVs), Copy Number Variations (CNVs) and Mitochondrial Heteroplasmy (MITO).