Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs565021665 1 159313100 downstream gene variant TTTTTTTTTTTTTT/-;TTTTT;TTTTTTT;TTTTTTTT;TTTTTTTTT;TTTTTTTTTT;TTTTTTTTTTT;TTTTTTTTTTTT;TTTTTTTTTTTTT;TTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTT delins 7.4E-02 1
rs35163651 6 41086523 intron variant TTTT/-;TTT;TTTTT;TTTTTT delins 1
rs34208856 6 135099930 intron variant TT/-;T;TTT;TTTTTTTTT delins 6
rs34687215 1 224394506 intron variant TT/-;T;TTT;TTTTT;TTTTTT;TTTTTTT delins 0.19 1
rs140740457 11 122629782 regulatory region variant TT/-;T;TTT;TTTTT delins 0.13 1
rs397731840 8 129599504 intron variant TT/-;T;TTT;TTTT;TTTTT delins 5
rs74267027 17 16268374 intron variant TT/- delins 0.40 3
rs146318841 6 135328483 intron variant TGCCATAAACCATAGCCATAG/-;TGCCATAAACCATAGCCATAGTGCCATAAACCATAGCCATAG delins 4
rs139707092 2 168850753 intron variant TCTCTGGAAT/-;TCTCTGGAATTCTCTGGAAT delins 5
rs138171347 17 5279909 upstream gene variant TAAA/-;TAAATAAA delins 1
rs78378222 0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 37
rs9260620 6 29955314 upstream gene variant T/G snv 0.24 7
rs2785663 1.000 0.040 1 157650968 intergenic variant T/G snv 0.64 2
rs3557 1 161219103 3 prime UTR variant T/G snv 6.5E-02 2
rs6846071 4 101481058 intron variant T/G snv 0.15 2
rs10840291 11 9708594 intron variant T/G snv 0.34 1
rs11602323 11 122648573 regulatory region variant T/G snv 0.14 1
rs117342529 8 21853230 intergenic variant T/G snv 2.6E-02 1
rs12074934 1 159338281 intergenic variant T/G snv 0.19 1
rs12144133 1 10144128 intron variant T/G snv 0.37 1
rs12740969 1 154514584 intron variant T/G snv 0.50 1
rs17038861 2 37006122 intron variant T/G snv 0.18 1
rs1997814 20 10666023 intron variant T/G snv 0.73 1
rs2227336 17 40018602 upstream gene variant T/G snv 0.36 1
rs2247584 1 159289890 intron variant T/G snv 0.34 1