Variant #0001267502 (NC_000013.10:g.19323853G>A)

Chromosome	13
DNA change (genomic) (Relative to hg19 / GRCh37)	g.19323853G>A
Reference	Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID	chr13_000002
Frequency	332/4566
Freq. EA	303/3182
Freq. AA	29/1384
Average frequency (gnomAD v.2.1.1)	-
Database submission license
Created by	Ivo F.A.C. Fokkema
Date created	2013-05-03 16:41:01 +02:00 (CEST)
Date last edited	N/A

Whole genome datasets