# Genes for Good v1.2.1: filtered, imputed genotype calls. For more information, go to: https://genesforgood.sph.umich.edu/readme/readme1.2.1.txt
# This data file generated by PLINK on: 11/20/17
#
# Below is a text version of your data.  Fields are TAB-separated.
# Each line corresponds to a single SNP.  For each SNP, we provide its
# identifier, its location on a reference human genome, and the genotype call.
# Human genome reference used: GRCh37/Mito:rCRS
#
# rsid	chromosome	position	genotype
rs3131970	1	753425	CC
rs3131969	1	754182	GG
rs3115858	1	755890	TT
rs3131962	1	756604	GG
rs114111569	1	759837	AA
rs1048488	1	760912	TT
rs75333668	1	762320	CC
rs2519025	1	765028	CC
rs4422949	1	834928	AG
rs72890788	1	836924	GA
rs12913832	15	28365618	AG # HERC2
rs80358622	13	32316497	AG # BRCA2 heterozygous variant
rs73885319	22	36661906	AG # APOL1 test entries (G1 het + G2 het)
rs60910145	22	36662034	TG # APOL1 test entries (G1 het + G2 het)
rs71785313	22	36662046	ID # APOL1 test entries (G1 het + G2 het)
rs143830837	22	36662046	ID # APOL1 test entries (G1 het + G2 het)
