DNA Marker Index information for Chromosome: Y Marker: FT76699.2
Names and Aliases for this DNA Marker: FT76699.2, rs959004346.
Chromosome Position in hg38 Human Genome assembly1: 15102999.
Chromosome Position in hg19 assembly2: 17214879 .
Ancestral marker allele value: G.
Derived, alternative, or mutated marker allele value: A.


DNA Marker Index data for Marker: FT76699.2 on Chromosome: Y
Marker Name(s) Notes Identification Ancestral7 Derived8 Chromosome Position (hg38)1 Position (hg19)2
FT76699.2 rs959004346
 Found in haplogroup R1b. See also FT76699.1 in haplogroup E1b.
DNA lineage FT76699.2 is estimated to have originated in about the year 120 bce based on its position in the phylogenetic tree.
Coincident with BY2574. 
View Ancestry 
NIH DBSNP b153 GRCh38p12 ClinVar? Position hg18: 15724273 		FTDNA 2019
G
A
Y
 15102999
17214879

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