Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800587 0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs3783553 0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs17561 0.672 0.560 2 112779646 missense variant C/A snv 0.27 0.26 23
rs2856836 0.763 0.280 2 112774506 3 prime UTR variant A/G snv 0.26 9
rs3783521 0.807 0.200 2 112786000 upstream gene variant G/A snv 0.26 8
rs3783546 0.882 0.160 2 112777253 intron variant G/C snv 0.70 5
rs3783550 0.827 0.200 2 112775308 intron variant G/T snv 0.64 0.70 5
rs2856838 0.851 0.200 2 112782395 intron variant G/A snv 0.37 4
rs1304037 0.882 0.200 2 112774659 3 prime UTR variant T/C snv 0.32 3
rs1609682 0.882 0.160 2 112782628 intron variant G/T snv 0.70 3
rs113129609 0.925 0.080 2 112778091 missense variant A/G snv 2
rs1516792 0.925 0.080 2 112778356 intron variant G/A snv 2
rs16347 0.925 0.080 2 112774138 3 prime UTR variant -/TGAA delins 0.70 2
rs1894399 0.925 0.040 2 112782600 intron variant C/T snv 0.32 2
rs1800794 1.000 0.040 2 112785696 upstream gene variant G/A snv 0.22 1
rs2071373 1.000 2 112782507 intron variant G/A snv 0.74 1
rs2071374 1.000 0.120 2 112779775 intron variant T/G snv 0.27 1
rs2071375 1.000 0.080 2 112777861 intron variant C/T snv 0.26 1
rs3783525 1.000 0.040 2 112784242 intron variant T/A;C snv 1