Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1015164
CCRL2
0.925 3 46410189 intron variant A/C;G;T snv 8
rs7691759 0.882 0.120 4 9686390 intron variant T/A;C snv 7
rs113974007 1.000 1 244750932 intergenic variant T/C snv 7.3E-02 5
rs11933652 1.000 4 28961215 intergenic variant T/C snv 0.12 5
rs13391004 1.000 2 136609937 intergenic variant G/A snv 9.1E-02 5
rs17841547 1.000 16 35734888 upstream gene variant A/C;G snv 5
rs2516928 1.000 14 106587377 upstream gene variant C/T snv 7.3E-02 5
rs2662411 1.000 5 10133592 upstream gene variant G/A;C snv 5
rs2801270 1.000 21 13297803 intergenic variant A/G snv 7.8E-02 5
rs28508297 1.000 14 106125683 upstream gene variant G/C snv 8.8E-02 5
rs28711761 1.000 8 6894170 downstream gene variant A/G snv 8.3E-02 5
rs35290534 1.000 4 187219164 regulatory region variant T/C snv 0.43 5
rs56775982 1.000 8 54303623 regulatory region variant C/T snv 8.5E-02 5
rs57989216 1.000 6 31368014 intron variant G/A snv 3.2E-02 5
rs5993499 1.000 22 16587858 downstream gene variant C/T snv 6.8E-02 5
rs60463810 1.000 6 148588135 intergenic variant C/T snv 0.12 5
rs6585943 1.000 10 85322237 intergenic variant G/A snv 0.41 5
rs7219088 1.000 17 41746019 intergenic variant T/C snv 0.60 5
rs7250377 1.000 19 32543335 intergenic variant G/T snv 9.9E-02 5
rs72847487 1.000 3 30504455 regulatory region variant C/T snv 9.0E-02 5
rs7697101 1.000 4 22173148 intron variant T/C snv 0.59 5
rs8094014 1.000 18 5940342 intron variant A/G snv 0.14 5
rs9688730 1.000 6 33957119 intergenic variant A/C snv 6.5E-02 5
rs9975780 1.000 21 26678731 intergenic variant C/T snv 0.10 5
rs9992616 1.000 4 56781880 intergenic variant C/A;G snv 5