Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1000778 1.000 0.040 11 61887833 intron variant A/G snv 0.59 3
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 8
rs10033601 1.000 0.040 4 152330909 intron variant A/G snv 0.37 0.42 1
rs1004467 0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 13
rs1004638 1.000 0.040 9 22115590 intron variant A/C;T snv 3
rs1007888 0.882 0.120 22 23898914 non coding transcript exon variant C/T snv 0.46 4
rs1008949 1.000 0.040 8 22696108 intron variant T/A;C;G snv 1
rs10093110 1.000 0.040 8 105553186 intron variant G/A;T snv 1
rs1010 0.807 0.120 2 85581859 3 prime UTR variant T/C;G snv 7
rs10106652 1.000 0.040 8 20070649 intergenic variant G/A snv 0.29 3
rs10116253 0.851 0.120 9 117702042 upstream gene variant T/C snv 0.28 4
rs10116277 0.827 0.160 9 22081398 intron variant G/T snv 0.62 8
rs10118757 0.827 0.120 9 21853340 intron variant A/G snv 0.26 7
rs10128951 1.000 0.040 12 124855901 intron variant G/A snv 0.47 1
rs10131519 1.000 0.040 14 99892957 intron variant T/C snv 0.29 1
rs10131894 1.000 0.040 14 74980176 regulatory region variant C/G snv 0.49 2
rs10139550 1.000 0.040 14 99679373 3 prime UTR variant C/G snv 0.39 1
rs10159239 0.882 0.040 1 247443750 intron variant G/A snv 0.57 3
rs1018383 1.000 0.040 6 11784092 intron variant C/T snv 0.76 1
rs10186133 1.000 0.040 2 113079367 downstream gene variant G/A;T snv 1
rs1020608562 0.807 0.160 3 46373738 missense variant T/C snv 4.0E-06 9
rs10221742 1.000 0.040 2 21196778 downstream gene variant G/A snv 0.32 1
rs10237377 1.000 0.040 7 140057336 intron variant G/T snv 0.48 1
rs1024610 0.882 0.200 17 34253212 upstream gene variant T/A snv 0.85 3
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63