2. Shon Robert EDWARDS [scrapbook] 1, 2, 3, 4 was born 5, 6, 7, 8 on 25 Jun 1966 in Salt Lake City, Salt Lake, Utah, United States. Shon was born in the covenant. He was baptized 9, 10 on 06 Jul 1974 in Normal, McLean, Illinois, United States. He was confirmed a member of The Church of Jesus Christ of Latter-day Saints on 06 Jul 1974 in Normal, McLean, Illinois, United States. He received his initiatory on 10 Jul 1985 in the Provo Utah temple. He was endowed 9 on 10 Jul 1985 in the Provo Utah temple. Shon married 11, 12, 13, 14, 15 Roya Michelle FARVID 16, 17, 18 on 01 Apr 1994 in Logan Temple, Logan, Cache, Utah, United States. They were sealed 19 on 01 Apr 1994 in the Logan Utah temple.
Long Count Date: LCD 12.17.12.14.19. Shon Robert EDWARDS was given a patriarchal blessing on 23 Aug 1981 in Provo, Utah, Utah, United States by . Shon Robert EDWARDS was ordained to the priesthood office of Elder on 22 Jul 1984 by . He served a mission from 16 Jan 1986 to 01 Jan 1988 in England, United Kingdom, Bristol Mission. He was blessed on 05 Mar 1999 in Salt Lake City, Salt Lake, Utah, United States by Neal A. Maxwell, Apostle. Shon was the ward communication specialist in the Chelsie Park 1st Ward, Layton West Stake from 08 Nov 2009 to 23 Aug 2020. Shon was the Ward Assistant Clerk--Membership in the Chelsie Park 1st Ward, Layton West Stake from 24 Sep 2017 to 23 Aug 2020. Shon was the FH Consultant in the Chelsie Park 1st Ward, Layton West Stake from 01 Jan 2023 to . [Parents]
ADDRESS/PHONE: old: 544 W. 600 N., #7; Provo, UT 84601/[1] (801) 344-6089.
New: 1039 N 2575 W, Layton, UT 84041-7709 +1 (801) 444-3445.FamilyTreeDNA kit #: 338036, password: sachsen
https://www.familytreedna.com/login.aspx
Autosomoal test indicates origins of Shon Edwards: 84% British Isles, 9% Eastern Europe, 8% (specifically Poland, Lithuania, Belarus, Czech Republic, Hungary, Romania); Southern Europe (specifically Portugal, Spain, Italy). A Y Chromosome test from descendants of James Newberry indicates American Indian ancestry for me: Cherokee and another tribe from the Great Lakes region.FamilyTreeDNA test #121898, haplotype I1 OR RATHER I-M253
DYS385A 13
DYS385B 14
DYS388 14
DYS389-1 13
DYS389-2 29
DYS390 22
DYS391 11
DYS392 11
DYS393 13
DYS394 14
DYS426 11
DYS437 16
DYS438 10
DYS439 11
DYS442 12
DYS444 11
DYS447 23
DYS448 20
DYS449 28
DYS454 11
DYS455 8
DYS456 14
DYS458 16
DYS459A 8
DYS459B 9
DYS460 11
DYS464A 12
DYS464B 14
DYS464C 15
DYS464D 15
DYS570 19
DYS576 18
DYS607 14
GATA-H4 11
YCA II A 19
YCA II B 22
CDY A 35
CDY B 38
, SRE, 24 Jun 2008.mtDNA test: THERE IS A LATER, MORE COMPREHENSIVE TEST LISTED AFTER THIS ONE
Testing company: SMGF (now AncestryDNA)
30 Nov 2002
SMGF-GF4609*
Haplogroup N9b/or probably more accurately with exact match H2a2a1
DELETED BY ANCESTRYDNA IN CA. 2013-2014. I WAS NOT WARNED IN ADVANCE.HVR1 mutations
16129AG
16223CT
16391AG
16519CTHVR2 mutations
00309.1C
00309.2C
00315.1COrigins are: Iceland, Faroe Islands, Finland, Japan, SE Asia, just north of Israel and including northern Israel. For H2a2a1, Scandinavia, Ireland, Germany, Europe in general, the Caucasus.
Also tried this web site and plugged in my numbers: https://dna.jameslick.com/mthap/mthap.cgi
Best mtDNA Haplogroup Matches:
1) H2a2a1
Defining Markers for haplogroup H2a2a1:
HVR2:
CR:
HVR1:Marker path from rCRS to haplogroup H2a2a1 (plus extra markers):
H2a2a1(rCRS) ? (309.1C) (309.2C) (315.1C)Perfect Match! Your results are an exact match to this haplogroup.
Extras(0): (309.1C) (309.2C) (315.1C)Gotten at discout for sample submitted to SMGF.ORG several years ago. Haplogroup N, subgoup N9b. Prevalent in Iceland, Lappland, Israel, and Southeast Asia. Haplogroups M and N, appearing about 63,000 years ago, represent two branches of haplogroup L3. Haplogroups M and N encompass the entire mitochondrial genetic pool of all non-African populations.
Approximately 60,000 years ago, haplogroup N diverged, giving rise to haplogroup R.
Phylogeography of M, N, and R
All over Eurasia, America, Australasia and Oceania, descendants of haplogroups M, N and R can be found, with only a few regional exceptions. The very similar ages of these three haplogroups indicate they were part of the same colonization process. This most likely involved the exodus of a small group of several hundred individuals from East Africa following the appearance of haplogroup L3. Subsequently, a period of variation occurred during which haplogroups M, N, and R evolved and the ancestral L3 was lost. Therefore, these three root types (which originated somewhere between East Africa and the Persian Gulf) must have been the founders for the settlement of Eurasia. Not only are the descendants of these founders ubiquitous outside of Africa, but their numerous sub-branches are also more specific to major geographic regions.
There is growing evidence that the richest variation in the three founder haplogroups M, N and R is found along the southern stretch of Eurasia, particularly the Indian subcontinent. Recent scientific findings suggest these haplogroups rapidly migrated along the southern coast of Asia. An analysis of western, southern, and eastern Eurasian and Australasian maternal lineages suggests a very short gradient of arrival times to these regions from about 66,000 years ago in India to about 63,000 years ago in Australasia, at a dispersal rate of about 4 km/year (2 ½ mi/year). Firm minimum archaeological age estimates are somewhat more recent (about 50,000 years for Australia and about 45,000 years for Southeast Asia), but evidence supporting earlier migrations may have been lost due to the rise of sea levels.
The expansions of haplogroups M, N and R northward to fill the heartland of the Eurasian continent started about 45,000 years ago, leaving a greater archaeological signature on the landscape as the population grew in size with improvement in technology and climatic conditions. This expansion, in turn, enabled the exploration and colonization of the interior of Eurasia. While haplogroups M, N, R and their branches are found throughout southern Asia, eastern Eurasia and Australasia, only high level haplogroup diversity within N and R are found in western Eurasia.
References
Macaulay V, Hill C, Achilli A, Rengo C, Clarke D, Meehan W, Blackburn J, Semino O, Scozzari R, Cruciani F, Taha A, Shaari NK, Raja JM, Ismail P, Zainuddin Z, Goodwin W, Bulbeck D, Bandelt HJ, Oppenheimer S, Torroni A, Richards M. Single, rapid coastal settlement of Asia revealed by analysis of complete mitochondrial genomes. Science. 2005 May 13;308(5724):1034-6.
