DNA Marker Index information for Chromosome: Y Marker: BY169952
Names and Aliases for this DNA Marker: BY169952.1, BY169952, rs771337154, BY169952.2, BY169952.3.
Chromosome Position in hg38 Human Genome assembly1: 12434175.
Chromosome Position in hg19 assembly2: 14545974 .
Ancestral marker allele value: G.
Derived, alternative, or mutated marker allele value: A.


DNA Marker Index data for Marker: BY169952 on Chromosome: Y
Marker Name(s) Notes Identification Ancestral7 Derived8 Chromosome Position (hg38)1 Position (hg19)2
BY169952.1 BY169952 rs771337154
 Found in haplogroup R1b under U106 with FTC18681 on FTDNA tree. See also BY169952.2 in haplogroup R1a. See also BY169952.3 in haplogroup R1b under M222. See also FTC9837 with different mutation at same position.
DNA lineage BY169952.1 is estimated to have originated in about the year 1,050 ce based on its position in the phylogenetic tree.
Coincident with FTC18681. 
View Ancestry 
NIH DBSNP b153 GRCh38p12 ClinVar? Position hg18: 13055982 		FTDNA 2018
G
A
Y
 12434175
14545974
BY169952.2 rs771337154
 Found in haplogroup R1a on academic study. See also BY169952.1 in haplogroup R1b under U106. See also BY169952.3 in haplogroup R1b under M222.
DNA lineage BY169952.2 is estimated to have originated in about the year 40 ce based on its position in the phylogenetic tree.
Coincident with A24888. 
View Ancestry 
NIH DBSNP b153 GRCh38p12 ClinVar? Position hg18: 13055982 		Academic List 2021
G
A
Y
 12434175
14545974
R-BY169952 
BY169952.3 rs771337154
 Found in haplogroup R1b under M222 and BY171768 on FTDNA tree. See also BY169952.1 in haplogroup R1b under U106. See also BY169952.2 in haplogroup R1a.
DNA lineage BY169952.3 is estimated to have originated in about the year 780 ce based on its position in the phylogenetic tree.
Phylogenetic Parent: BY171768 
View Ancestry 
Phylogenetic Children: BY169837 
NIH DBSNP b153 GRCh38p12 ClinVar? Position hg18: 13055982 		FTDNA 2023
G
A
Y
 12434175
14545974

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