Join Our Rare Disease Day Special Initiative

[Sequencing.com]

Get 85% Off + Free Upgrade To Expedited Processing

[Rare Disease Day Special Offer](https://links.dna.sequencing.com/web-only/z/oykgkff33?uid=b5dd70e0-a350-4d06-ac9b-9ae02ff7deb8&txnid=c0053084-fd7e-489d-8c08-a03ef18f65d3&mid=5bfdbc45-053c-4f36-89de-04cdd345bb80&bsft_ek=2024-02-16T17%3A05%3A21Z&bsft_mime_type=text&bsft_tv=10&bsft_lx=1)

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Join Our Rare Disease Day Initiative

Sequence Your Genome, Help A Family In Need

In honor of Rare Disease Day, we invite you to be part of a special initiative: for every 50 Rare Disease Day WGS Special Bundles ordered, we pledge to donate a bundle to a family grappling with unresolved health mysteries. These families in need stand to gain invaluable insights from genome sequencing, offering them a beacon of hope in their search for answers.

When you order a Rare Disease Day Bundle, you're doing more than sequencing your own genome; you're contributing to a lifeline for families facing their most challenging times.

[Support Rare Disease Day](https://links.dna.sequencing.com/z/oykgkff33?uid=b5dd70e0-a350-4d06-ac9b-9ae02ff7deb8&txnid=c0053084-fd7e-489d-8c08-a03ef18f65d3&mid=5bfdbc45-053c-4f36-89de-04cdd345bb80&bsft_ek=2024-02-16T17%3A05%3A21Z&bsft_mime_type=text&bsft_tv=10&bsft_lx=3)

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Rare Disease Day Special Bundle

WGS + Our Best Reports + Expedited Processing

Embrace this unique opportunity with our Rare Disease Day WGS Special Bundle. This comprehensive bundle includes Whole Genome Sequencing and 10 DNA health reports. It also includes a free upgrade to Expedited Processing that delivers results up to 50% faster.

Bundle Includes:

- Whole Genome Sequencing DNA Kit
- Free Worldwide Shipping
- Expedited Laboratory Processing
- Next-Gen Disease Screen (analyzes 15,000+ conditions)
- 10 DNA Health Reports
- Lifetime DNA Storage
- Privacy Forever Data Protection
- Industry-Leading Customer Support
- Access To 100+ DNA Reports

[Get My Disease Screen](https://links.dna.sequencing.com/z/oykgkff33?uid=b5dd70e0-a350-4d06-ac9b-9ae02ff7deb8&txnid=c0053084-fd7e-489d-8c08-a03ef18f65d3&mid=5bfdbc45-053c-4f36-89de-04cdd345bb80&bsft_ek=2024-02-16T17%3A05%3A21Z&bsft_mime_type=text&bsft_tv=10&bsft_lx=6)

 

Our Founder's Rare Disease Journey

https://links.dna.sequencing.com/z/oykgkff33?uid=b5dd70e0-a350-4d06-ac9b-9ae02ff7deb8&txnid=c0053084-fd7e-489d-8c08-a03ef18f65d3&mid=5bfdbc45-053c-4f36-89de-04cdd345bb80&bsft_ek=2024-02-16T17%3A05%3A21Z&bsft_mime_type=text&bsft_tv=10&bsft_lx=7

Decades of inconclusive tests marked Dr. Brandon Colby's quest to understand his rare disease—a journey that ended with the discovery of a mutation in his KRT14 gene, thanks to our Whole Genome Sequencing service combined with our Next-Gen Disease Screen (NGDS).

This pivotal breakthrough not only unveiled long-awaited answers for Dr. Colby but also showcased the groundbreaking capabilities of NGDS in offering essential genetic insights other tests failed to detect. Influenced deeply by his own experience, Dr. Colby has steered Sequencing's mission towards empowering everyone to be able to outsmart their genes.

[Read About Dr. Colby's Journey](https://links.dna.sequencing.com/z/oykgkff33?uid=b5dd70e0-a350-4d06-ac9b-9ae02ff7deb8&txnid=c0053084-fd7e-489d-8c08-a03ef18f65d3&mid=5bfdbc45-053c-4f36-89de-04cdd345bb80&bsft_ek=2024-02-16T17%3A05%3A21Z&bsft_mime_type=text&bsft_tv=10&bsft_lx=8)

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