DNA Marker Index information for Chromosome: Y Marker: L669
Names and Aliases for this DNA Marker: L669.1, L669, L669.2, L669.3, rs368818579, L669.4.
Chromosome Position in hg38 Human Genome assembly1: 6885250.
Chromosome Position in hg19 assembly2: 6753291 .
Ancestral marker allele value: G.
Derived, alternative, or mutated marker allele value: C.


DNA Marker Index data for Marker: L669 on Chromosome: Y

Marker Name(s) Notes Identification Ancestral7 Derived8 Chromosome Position (hg38)1 Position (hg19)2
L669.1 L669 rs368818579
Found in haplogroup R1a under M417. See also L669.2 in haplogroup J2b. See also L669.3 in haplogroup O2a. See also L669.4 in haplogroup C. See also L685 with different mutation at same position. See also L1242 with different mutation at same position.

NIH DBSNP b153 GRCh38p12 ClinVar? Position hg18: 6813291
Thomas Krahn, FTDNA
G
C
Y
6885250
6753291
L669.2 rs368818579
Found in haplogroup J2b with BY130638. See also L669.1 in haplogroup R1a. See also L669.3 in haplogroup O2a. See also L669.4 in haplogroup C.
DNA lineage L669.2 is estimated to have originated in about the year 33,700 bce based on its position in the phylogenetic tree.

Coincident with BY130638
View Ancestry 

NIH DBSNP b153 GRCh38p12 ClinVar? Position hg18: 6813291
Thomas Krahn, YSeq
G
C
Y
6885250
6753291
L669.3 rs368818579
Found in haplogroup O2a with MF32740 on 23mofang tree. See also L669.1 in haplogroup R1a. See also L669.2 in haplogroup J2b. See also L669.4 in haplogroup C.
DNA lineage L669.3 is estimated to have originated in about the year 10 bce based on its position in the phylogenetic tree.

Coincident with MF32740
View Ancestry 

NIH DBSNP b153 GRCh38p12 ClinVar? Position hg18: 6813291
23mofang 2023
G
C
Y
6885250
6753291
L669.4 rs368818579
Found in haplogroup C root with M130 on 23mofang tree. See also L669.1 in haplogroup R1a. See also L669.2 in haplogroup J2b. See also L669.3 in haplogroup O2a.
DNA lineage L669.4 is estimated to have originated in about the year 63,400 bce based on its position in the phylogenetic tree.

Coincident with M216
View Ancestry 

NIH DBSNP b153 GRCh38p12 ClinVar? Position hg18: 6813291
23mofang 2023
G
C
Y
6885250
6753291

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