Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs1801260 0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs76863441 0.672 0.440 6 46709361 missense variant C/A snv 4.5E-03 1.3E-03 25
rs505151 0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 18
rs55951658 0.827 0.200 7 99770202 missense variant T/A;C snv 4.1E-04 9.8E-05 7
rs619203 0.851 0.160 6 117301021 missense variant G/C snv 0.20 0.19 6
rs768925824 0.925 0.040 19 11110693 missense variant G/A snv 4.0E-06 4