App chain |
Chain# | Description |
|---|---|---|
| Von Willebrand Disease, Type 2B | Chain45 | Determine predisposition to bleeding disorder |
| Von Willebrand Disease, Type 1 | Chain44 | Determine predisposition to bleeding disorder |
| Von Hippel-Lindau Syndrome | Chain1591 | This is a rare disease. |
| Vohwinkel Syndrome | Chain1590 | This is a rare disease. |
| Vitelliform Macular Dystrophy | Chain1589 | This is a rare disease. |
| Vitamin K-Dependent Coagulation Defect | Chain1588 | This is a rare disease. |
| Vitamin D-dependent Rickets, Type I | Chain1587 | This is a rare disease. |
| Vitamin D supplements more likely to benefit health | Chain88 | Determine the optimal level of Vitamin D |
| Vitamin D Affinity | Chain1586 | This is a rare disease. |
| Visual Hallucinations and Hyperphagia with Alzheimer Disease | Chain1585 | This is a rare disease. |
| Vesicoureteral Reflux | Chain1584 | This is a rare disease. |
| Venous Thromboembolism associated with Thalidomide | Chain1582 | This is a rare disease. |
| Venous Thromboembolism (Analysis B) | Chain1581 | This is a rare disease. |
| Venous Thromboembolism (Analysis A) | Chain1580 | This is a rare disease. |
| Venous Thromboembolic Disease | Chain1579 | This is a rare disease. |
| Usher Syndrome, Type III | Chain1575 | This is a rare disease. |
| Usher Syndrome, Type IIA | Chain1574 | This is a rare disease. |
| Usher Syndrome, Type 2C | Chain1573 | This is a rare disease. |
| Usher Syndrome, Type 1c | Chain1570 | This is a rare disease. |
| Usher Syndrome, Type 1b | Chain1569 | This is a rare disease. |
| Usher Syndrome, Type 1G | Chain1572 | This is a rare disease. |
| Usher Syndrome, Type 1F | Chain1571 | This is a rare disease. |
| Usher Syndrome 1 | Chain1568 | This is a rare disease. |
| Urea Transport Defect JK-Null Variant | Chain1567 | This is a rare disease. |
| Unna-Thost Disease | Chain1566 | This is a rare disease. |
| Universal Genetic Data API | Genotypes | If you previously used 23andMe's API, our Universal Genetic Data API will function in the same way (similar API calls, similar data structure). The Universal Genetic Data API will soon be available as part of Sequencing.com's Real-Time Personalization (+RTP) API. The Universal Genetic Data API will securely send your app genetic (genotypic) data. This includes the ability for your app to request and receive genotypes for predefined datasets (such as for all variants in the '23andMe v5 dataset') as well as the ability to request genotypes for specific variants by rsid or chromosomal coordinate (aligned to either hg19 or hg38). Regardless of the user's genetic data format, Sequencing.com's Universal Compatibility will always send your app genotypic data using the same data structure. Using our API, you'll be able to reach everyone in the world who has had a genetic test. This includes compatibility with genetic data generated by 23andMe, AncestryDNA, Helix, Family Tree DNA, MyHeritage, Dante Labs, Diagnomics, Living DNA, Vitagene, etc. as well as both exome and whole genome sequencing (WGS) from all laboratories (NIH's All of Us, Illumina's Clinical Lab, Macrogen, Fulgent, Novogene, WuXi NextCODE, BGI, LabCorp, Quest, etc.). |
| Unipolar Depression Depression Poorly Responsive or Unresponsive to SSRIs | Chain1565 | This is a rare disease. |
| UV-sensitive Syndrome | Chain1576 | This is a rare disease. |
| Tyrosinemia, Type III | Chain1564 | This is a rare disease. |
| Tyrosinemia, Type II | Chain1563 | This is a rare disease. |
| Tyrosinemia, Type I | Chain1562 | This is a rare disease. |
| Typical Migraine with Aura | Chain1561 | This is a rare disease. |
| Tumoral Calcinosis, Hyperphasphatemic, Familial | Chain1560 | This is a rare disease. |
| Tuberous Sclerosis | Chain1559 | This is a rare disease. |
| Tuberculoid Leprosy versus Lepromatous Leprosy | Chain1558 | This is a rare disease. |