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Archiver > GENEALOGY-DNA > 2008-02 > 1203882027


From: "Tim Janzen" <>
Subject: Re: [DNA] 23ANDme versus deCODEme
Date: Sun, 24 Feb 2008 11:40:27 -0800
In-Reply-To: <001301c8770a$1f0ea190$5d2be4b0$@rr.com>


Dear Eldon,
It would be very helpful if you were to share with us the rs numbers
and/or positions of the 10 Y SNPs that you also share with both Dr. Venter
and Dr. Watson. The 10 SNPs that you share with both Dr. Venter and Dr.
Watson may be important SNPs that define deep subclades that are downstream
from S21. I would also be interested in knowing the 4 SNPs that you share
with Dr. Venter only. Those SNPs are also likely to be important and
probably define deep subclades. The 132 SNPS that Dr. Venter and Dr. Watson
share are at
http://freepages.genealogy.rootsweb.com/~ncscotts/Y-DNA/Tim%20Janzen/W_V-sha
red-SNPs.htm. As you may recall we had extensive discussion of their SNPs
on this list in December and January.
Sincerely,
Tim Janzen

-----Original Message-----
From:
[mailto:] On Behalf Of Eldon Wade
Sent: Sunday, February 24, 2008 9:25 AM
To:
Subject: Re: [DNA] 23ANDme versus deCODEme

David,

I tested with deCODEme. Of their 1,071,000 targeted SNPs I received results
on 1,013,349. Of these, 162 were mtDNA, 858 were Y-SNPs, 36,589 were
X-SNPs, and 975,740 were autosomal SNPs.

When comparing my 858 Y-SNPs to the HUGO reference there were 28 variations.
10 of these variations I shared with both Dr. Venter and Dr. Watson who are
also R1b1c9. I have 4 variations I share with Dr. Venter only. Thus I have
14 variations that I do not share with either Dr. Venter or Dr. Watson.

Eldon


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