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
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs34637584 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs5569 0.742 0.280 16 55697923 synonymous variant G/A;C snv 0.31; 4.0E-06 19
rs2283265 0.776 0.160 11 113414814 intron variant C/A snv 0.16 12
rs75634836 0.807 0.160 13 46835532 missense variant C/A;T snv 4.0E-06 11
rs1800035 0.925 0.080 10 111078794 missense variant C/G;T snv 1.9E-03 4