DNA Marker Index information for Chromosome: Y Marker: FGC10543.2
Names and Aliases for this DNA Marker: FGC10543.2, rs1026763613.
Chromosome Position in hg38 Human Genome assembly1: 16985046.
Chromosome Position in hg19 assembly2: 19096926 .
Ancestral marker allele value: G.
Derived, alternative, or mutated marker allele value: A.


DNA Marker Index data for Marker: FGC10543.2 on Chromosome: Y
Marker Name(s) Notes Identification Ancestral7 Derived8 Chromosome Position (hg38)1 Position (hg19)2
FGC10543.2 rs1026763613
 Found in haplogroup T1a under Y45975 on YFull tree. Believed coincident with Y45545 on FTDNA tree. Example is YF004504 from Bahrain. See also FGC10543.1 in haplogroup R1b under U152. See also FGC10543.3 in haplogroup R1b under ZZ29. See also FGC10543.4 in haplogroup R1b under M222.
DNA lineage FGC10543.2 is estimated to have originated in about the year 4,180 bce based on its position in the phylogenetic tree.
Coincident with Y45545. 
View Ancestry 
NIH DBSNP b153 GRCh38p12 ClinVar? Position hg18: 17606320 		YFull 2021
G
A
Y
 16985046
19096926

Links for more information