Skip to main content

Another test or website gave me a completely different haplogroup, a different main branch — which is right?

Why calls can differ across tools, what a different main branch usually means, and how to send us your file for review.

Calls can differ across tools because they read different positions, use different reference trees, and make different calls on low-coverage data. A different main branch (not just a deeper twig) usually points to a coverage or calling difference. We place you only on branches your markers clearly support; if you’d like, you can send your file to our team for a manual review.

Still stuck? If you have a Genomelink account, head to genomelink.io/profile/contact and message us from the form — we can help faster when we can see your account. New and don't have an account yet? Email us at info@genomelink.io and we'll sort it out.

Did this answer your question?