Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12041331 0.776 0.200 1 156899922 intron variant G/A snv 0.19 11
rs5050
AGT
0.827 0.200 1 230714140 intron variant T/C;G snv 7
rs2229634 0.851 0.240 6 33670403 synonymous variant C/A;T snv 4.0E-06; 0.33 4
rs16921209 0.882 0.160 10 20879174 intron variant C/G snv 4.6E-02 3
rs17076896 0.882 0.160 13 19181923 upstream gene variant T/C snv 8.3E-02 3
rs7637803 0.882 0.160 3 151371438 intron variant C/G;T snv 3
rs899162 0.882 0.160 5 135459219 downstream gene variant G/A snv 1.0E-01 3