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Subject: Post 259 A: Azariah = Khazaria


Author:
teltalheart/moderator
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Date Posted: 00:34:37 02/14/11 Mon
Author Host/IP: 98-159-200-219.scottsboro.org/98.159.200.219

Post 259 A: Azariah = Khazaria

Azariah was the son of Ahimaaz (1 Kings 4:2) and grandson of Zadok, the High Priest in the time of King David (II Sam. xv. 24-29; comp.35).

Khazaria is the region between the Black Sea and the Caspian Sea. It is the area already mentioned in Post 258. It is also the area many writers and scholars have proposed as the true homeland and beginning of the Jewish race. One wonders if Azariah didn't lend his name to this region. I personally wonder if most of the story of the Old Testament didn't take place in this region instead of the supposed "holy land."

As was discussed in Post 258 there really is no specific "Hebrew DNA." However there are DNAs that are most often found among the Jews. they are as fallows: Haplogroups G, J, L, T, and E. But one may have one of these haplogroups and not be a Jew at all. Then again it might show a heritage from a distant ancestor who was a member of the race of people that became known as the Hebrews.

The Y-DNA is as follows with the amount or number of thousands of years ago each came into being and migrated:
A 60, B50, CT 50, D 50, E 50, E1b1a 20, E1b1b 20, C 50, F 45, G 20, H 30, I 25, J 25, K 40, L 30, M 10, N 10, O 35, O3 35, P 35, Q 20, Q1a3a 10, R 30, R1a 10, R1b 25, S 10, T 10.

A, B, D, E, and C are usually the oldest "out of Africa" DNAs. F, G, H, I, J, and K are usually Middle Eastern and Near Eastern DNAs. R is most often found in Western Asia and Europe. This is, however, a gross generalization.

I do not know about all the factors of all the DNA groups. But I do know a little about J. It seems the phenotype of mtDNA J persons produce higher body heat. This is why it's thought this group can be found in northern Europe, particularly in Norway.
Also as one report put it: "The T150C mutation, which is exclusive to but not definitive of, the J2 subclade of Haplogroup J. May be part of a likely nuclearly controlled general machinery regarding the remodeling and replication of mtDNA. Controlling a remodeling which could accelerate mtDNA replication thus compensation for oxidative damage in mtDNA as well as functional deterioration occurring with old age related to it."- (A Comprehensive Analysis of mtDNA Haplogroup J, - Jim Logan. September, 2008).

End Post 259 A: www.voy.com/40560/ teltalheart

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