DNA Marker Index information for Chromosome: Y Marker: FGC10790.2
Names and Aliases for this DNA Marker: FGC10790.2, Y3037.2, rs781653170.
Chromosome Position in hg38 Human Genome assembly1: 10053726.
Chromosome Position in hg19 assembly2: 9891335 .
Ancestral marker allele value: T.
Derived, alternative, or mutated marker allele value: C.


DNA Marker Index data for Marker: FGC10790.2 on Chromosome: Y
Marker Name(s) Notes Identification Ancestral7 Derived8 Chromosome Position (hg38)1 Position (hg19)2
FGC10790.2 Y3037.2 rs781653170
 Found in haplogroup R1b with BY56897 on FTDNA tree. See also Y3037.1 / FGC10790.1 in haplogroup N1a. See also Y3037.1 in haplogroup N1a.
DNA lineage FGC10790.2 is estimated to have originated in about the year 10 bce based on its position in the phylogenetic tree.
Coincident with BY56897. 
View Ancestry 
NIH DBSNP b153 GRCh38p12 ClinVar? Position hg18: 10501335 		FTDNA 2024
T
C
Y
 10053726
9891335

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