Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs199750 0.882 0.160 6 26016234 upstream gene variant C/T snv 0.77 5
rs4307059 0.882 0.080 5 25967594 intron variant T/A;C snv 5
rs2380205 0.882 0.080 10 5844771 upstream gene variant C/T snv 0.47 3
rs2597513 1.000 0.040 3 13514336 regulatory region variant C/T snv 0.88 3
rs4327572 0.882 0.120 5 25972712 intron variant C/T snv 0.28 3
rs6088343 1.000 0.040 20 33908259 downstream gene variant C/T snv 0.46 3
rs6142044 1.000 0.040 20 33918789 intergenic variant A/T snv 0.47 3
rs6489785 1.000 0.040 12 120925921 TF binding site variant T/C snv 0.68 3
rs10086987 1.000 0.040 8 47177908 intron variant G/A;C snv 2
rs1010053 0.925 0.080 14 60538907 intron variant A/G snv 0.34 2
rs10484432 1.000 0.040 6 26008648 upstream gene variant G/A snv 0.17 2
rs10484433 1.000 0.040 6 26030264 upstream gene variant C/A snv 9.6E-02 2
rs11224294 0.925 0.080 11 100578431 regulatory region variant T/C snv 9.9E-02 2
rs11264339 1.000 0.040 1 155168172 downstream gene variant C/T snv 0.56 2
rs11265022 1.000 0.040 1 158542829 downstream gene variant T/A snv 0.21 2
rs12094989 1.000 0.040 1 26521895 upstream gene variant C/T snv 0.29 2
rs13220395 1.000 0.040 6 26055140 downstream gene variant G/A;C snv 2
rs1409568 1.000 0.040 10 118871273 intron variant T/C snv 8.2E-02 2
rs1559715 1.000 0.040 4 54207506 intron variant G/A snv 0.20 2
rs16891264 1.000 0.040 6 26072217 intergenic variant T/C snv 9.0E-02 2
rs17399603 1.000 0.040 3 101017295 regulatory region variant A/G snv 0.10 2
rs2452877 1.000 0.040 5 4027643 regulatory region variant A/G snv 0.60 2
rs2726034 1.000 0.040 16 28325561 downstream gene variant T/C snv 0.37 2
rs2785663 1.000 0.040 1 157650968 intergenic variant T/G snv 0.64 2
rs2897047 0.925 0.040 5 2640009 regulatory region variant A/G snv 0.63 2