DNA Marker Index information for Chromosome: Y Marker: FGC6662.2
Names and Aliases for this DNA Marker: FGC6662.2, rs1035855309.
Chromosome Position in hg38 Human Genome assembly1: 13758449.
Chromosome Position in hg19 assembly2: 15870329 .
Ancestral marker allele value: C.
Derived, alternative, or mutated marker allele value: T.


DNA Marker Index data for Marker: FGC6662.2 on Chromosome: Y
Marker Name(s) Notes Identification Ancestral7 Derived8 Chromosome Position (hg38)1 Position (hg19)2
FGC6662.2 rs1035855309
 Found in haplogroup G2a. See also FGC6662.1 in haplogroup J2a. See also FGC6662.1 in haplogroup J2a. See also FGC6662.3 in haplogroup R.
DNA lineage FGC6662.2 is estimated to have originated in about the year 33,700 bce based on its position in the phylogenetic tree.
Coincident with FGC6622. 
View Ancestry 
NIH DBSNP b153 GRCh38p12 ClinVar? Position hg18: 14379723 		ISOGG 2020
C
T
Y
 13758449
15870329

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