Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs3087243 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 44
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 22
rs763361 0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 21
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs3733197 0.742 0.320 4 101918130 missense variant G/A snv 0.31 0.30 13
rs2900180 0.827 0.280 9 120944104 regulatory region variant T/A;C snv 5