Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1220579705
IL4
1.000 0.080 5 132674079 missense variant C/T snv 1
rs12570188 1.000 0.080 10 99095945 intron variant C/T snv 1.5E-02 1
rs12750027 1.000 0.080 1 212883085 intron variant G/A snv 4.3E-02 1
rs1314595 1.000 0.080 10 115148713 intron variant C/T snv 4.3E-02 1
rs1530976 1.000 0.080 4 71527674 intron variant G/A;C snv 1
rs16882243 1.000 0.080 5 9226328 intron variant C/G snv 1.2E-02 1
rs16925517 1.000 0.080 9 106484720 intron variant G/A;C snv 1
rs16929097 1.000 0.080 9 12521826 intergenic variant G/A snv 4.7E-02 1
rs17033506 1.000 0.080 3 35598334 intergenic variant G/T snv 2.8E-02 1
rs17111521 1.000 0.080 14 41164182 intergenic variant C/A snv 6.7E-02 1
rs1716183 1.000 0.080 12 123150549 upstream gene variant C/T snv 0.34 1
rs17218161 1.000 0.080 4 58347679 intergenic variant T/C snv 4.3E-03 1
rs1931704 1.000 0.080 10 127541545 intergenic variant G/A snv 0.28 1
rs2037986 1.000 0.080 21 28104158 intron variant G/T snv 0.44 1
rs2051809 1.000 0.080 5 132721182 intron variant A/C snv 0.58 1
rs2289447 1.000 0.080 1 46652496 non coding transcript exon variant C/G;T snv 1
rs2292527 1.000 0.080 17 17222727 non coding transcript exon variant G/A snv 3.6E-02 1
rs2311978 1.000 0.080 X 76568453 intergenic variant C/T snv 0.58 1
rs2313640 1.000 0.080 17 39955592 intron variant C/T snv 0.69 1
rs2378383 1.000 0.080 9 79424447 intergenic variant A/C;G;T snv 1
rs2928442 1.000 0.080 10 57386706 intergenic variant T/A;C snv 1
rs34104444 1.000 0.080 10 110885330 synonymous variant G/A snv 3.7E-02 6.0E-02 1
rs34880821 1.000 0.080 7 22735831 downstream gene variant G/A snv 0.21 1
rs35141484 1.000 0.080 4 39086721 synonymous variant A/C snv 5.6E-03 2.2E-02 1
rs3752120 1.000 0.080 19 52048768 5 prime UTR variant C/T snv 0.14 1