Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs146425640 1.000 11 19823052 intron variant A/C snv 2.8E-03 1
rs184429573 1.000 12 28504235 intron variant A/C snv 9.1E-03 1
rs190508378 1.000 21 31697608 intron variant A/C snv 3.4E-03 1
rs57997684 1.000 6 11014323 intron variant A/C snv 0.13 1
rs73184656 1.000 3 187724028 intron variant A/C snv 0.18 1
rs4767831 1.000 12 119601623 intron variant A/C;G snv 1
rs10505380 1.000 8 120314234 intron variant A/G snv 0.14 1
rs67134687 1.000 9 21845309 intron variant A/G snv 9.2E-02 1
rs7048567 1.000 9 137009585 synonymous variant A/G snv 0.68 0.70 1
rs75495219 1.000 10 67151138 intron variant A/G snv 6.0E-02 1
rs1882642 1.000 2 141104341 intron variant A/G;T snv 1
rs117451620 1.000 22 33873469 intron variant C/A snv 1.8E-02 1
rs76456255 1.000 12 65950114 intron variant C/A snv 6.5E-02 1
rs139465532 1.000 20 8348184 intron variant C/G snv 6.8E-03 1
rs142630661 1.000 11 71794579 non coding transcript exon variant C/G snv 1.3E-02 1
rs189131320 1.000 1 24951485 intron variant C/G snv 2.3E-03 1
rs114830967 1.000 2 115820465 intron variant C/T snv 2.0E-02 1
rs12118495 1.000 1 204077651 intron variant C/T snv 7.8E-02 1
rs12232685 1.000 18 13437028 intron variant C/T snv 4.8E-02 1
rs140255439 1.000 17 2638960 intron variant C/T snv 6.3E-02 1
rs142897541 1.000 2 192095144 intron variant C/T snv 1.6E-02 1
rs150859230 1.000 1 216675108 intron variant C/T snv 1.4E-02 1
rs151068302 1.000 9 26883048 intron variant C/T snv 6.1E-02 1
rs192597095 1.000 12 56486375 intron variant C/T snv 8.6E-03 1
rs72656469 1.000 8 64701356 intron variant C/T snv 1.9E-02 1