Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519723 0.925 0.120 9 5078362 missense variant A/C;G;T snv 1
rs1057519721 0.882 0.120 9 5078360 missense variant A/G snv 2
rs142269166 1.000 0.040 9 5126715 missense variant A/G snv 2.0E-03 2.1E-03 1
rs1479478620 1.000 0.040 9 5126768 missense variant A/G snv 1
rs2274471 1.000 0.040 9 4985879 intron variant A/G snv 0.21 1
rs59384377 1.000 0.080 9 5005034 intron variant A/T snv 0.26 1
rs121912473 0.925 0.080 9 5070026 missense variant AA/TT mnv 2
rs7046736 0.925 0.080 9 5015732 intron variant C/A snv 0.39 2
rs12340895 1.000 0.080 9 5076691 intron variant C/A;G snv 1
rs771912975 1.000 0.040 9 5055750 stop gained C/A;G;T snv 4.0E-06; 1.6E-05 1
rs1057520016 0.851 0.080 9 5089726 missense variant C/A;T snv 4
rs10974944 0.882 0.160 9 5070831 intron variant C/G snv 0.25 4
rs1339159756 0.925 0.120 9 5078395 missense variant C/G snv 2
rs7849191 0.882 0.120 9 4988761 intron variant C/T snv 0.50 2
rs1319313254 9 5050807 missense variant C/T snv 4.0E-06 1
rs3780378 1.000 0.040 9 5112288 non coding transcript exon variant C/T snv 0.51 1
rs2149556 1.000 0.080 9 5059440 intron variant C/T snv 0.64 1
rs2230724 0.851 0.120 9 5081780 synonymous variant G/A snv 0.53 0.62 4
rs10974947 0.882 0.080 9 5072846 intron variant G/A snv 0.23 3
rs10815144 0.882 0.080 9 5010192 intron variant G/A snv 0.62 3
rs777015472 1.000 0.040 9 5066740 missense variant G/A snv 1.2E-05 7.0E-06 1
rs1392759936 1.000 0.040 9 5054778 missense variant G/A snv 7.0E-06 1
rs1346944271 1.000 0.120 9 5090497 missense variant G/A snv 1.4E-05 1
rs56118985 0.882 0.080 9 5044432 missense variant G/A;C snv 1.8E-03; 4.0E-06 3
rs774709145 9 5080657 missense variant G/A;C snv 1.3E-05 1