Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10224002 0.925 0.080 7 151717955 intron variant A/G snv 0.31 12
rs1037733674 0.882 0.120 2 162147429 missense variant T/C snv 1.4E-05 5
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs10887800 0.790 0.280 10 88316086 intron variant A/G;T snv 11
rs11066280 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs11124945 1.000 0.040 2 43650017 intron variant A/G snv 0.21 3
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs113296370 1.000 0.040 2 43636315 upstream gene variant A/C snv 0.17 3
rs11575937 0.653 0.480 1 156136985 missense variant G/A;T snv 29
rs11712619 0.882 0.160 3 124300955 intron variant C/A;T snv 0.26 5
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 20
rs12579302 0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs12917707 0.827 0.200 16 20356368 upstream gene variant G/T snv 0.14 11
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs13333226 0.827 0.200 16 20354332 intron variant A/G snv 0.23 10
rs137853240 0.807 0.080 12 120994405 missense variant G/A snv 1.4E-05 8
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1570360 0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs17111503 0.925 0.160 1 55037775 upstream gene variant A/G snv 0.22 7
rs17249754 0.882 0.120 12 89666809 intron variant G/A snv 0.15 12
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74