DNA Marker Index information for Chromosome: Y Marker: L667.2
Names and Aliases for this DNA Marker: L667.2, M2226.1, M2226, CTS7551.1, CTS7551, rs557831756.
Chromosome Position in hg38 Human Genome assembly1: 15421375.
Chromosome Position in hg19 assembly2: 17533255 .
Ancestral marker allele value: G.
Derived, alternative, or mutated marker allele value: A.


DNA Marker Index data for Marker: L667.2 on Chromosome: Y
Marker Name(s) Notes Identification Ancestral7 Derived8 Chromosome Position (hg38)1 Position (hg19)2
G-L667 
L667.2 M2226.1 M2226 CTS7551.1 CTS7551 rs557831756
 Found in haplogroup G2a under FT39559 on FTDNA tree. Believed coincident with Y170316 on YFull tree. Example is YF019893 from Switzerland. See also L667.1 in haplogroup N.
DNA lineage L667.2 is estimated to have originated in about the year 2,770 bce based on its position in the phylogenetic tree.
Phylogenetic Parent: FT39559 
View Ancestry 
Phylogenetic Children: BY96577  FT43901 
NIH DBSNP b153 GRCh38p12 ClinVar? Position hg18: 16042649 		Underhill et al
G
A
Y
 15421375
17533255

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