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
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
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
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs8192678 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs4402960 0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs17446614 0.851 0.240 13 40565740 intron variant G/A snv 0.16 5