Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs713598 0.851 0.160 7 141973545 missense variant C/G snv 0.46 0.44 7
rs10246939 0.851 0.240 7 141972804 missense variant T/C snv 0.49 0.47 6
rs1726866 0.925 0.120 7 141972905 missense variant G/A snv 0.50 0.47 3
rs4725559
AGK
7 141587852 intron variant G/A snv 0.36 1
rs12539499 7 141930467 intron variant T/C snv 0.23 1
rs4726463 7 141666839 intron variant A/G snv 0.35 1
rs11762634 7 141956687 intron variant G/A snv 0.22 1
rs11767119 7 141912316 intron variant G/A snv 0.23 1
rs11767947 7 141912821 intron variant G/A snv 0.23 1
rs17162635 7 141978163 intron variant T/A snv 1.0E-01 1
rs4726481 7 141968603 intron variant G/T snv 0.43 1
rs6976028 7 141912917 intron variant C/T snv 0.25 1