Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs27432 0.925 0.040 5 96783569 intron variant A/C;G snv 2
rs4561177 0.807 0.120 11 110091706 intron variant A/G snv 0.36 6
rs694739 0.763 0.320 11 64329761 upstream gene variant A/G snv 0.28 6
rs7552167 0.807 0.120 1 24192153 upstream gene variant A/G snv 0.87 6
rs10865331 0.827 0.120 2 62324337 intergenic variant A/G snv 0.57 5
rs1295685 0.790 0.160 5 132660753 3 prime UTR variant A/G snv 0.81 4
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 4
rs2675662 0.925 0.040 10 73839369 intron variant A/G snv 0.55 2
rs27524 0.851 0.160 5 96766240 intron variant A/G snv 0.61 1
rs3135388 0.807 0.240 6 32445274 downstream gene variant A/G snv 0.90 1
rs3802826 0.925 0.040 11 128536543 non coding transcript exon variant A/G;T snv 2
rs7637230 0.925 0.040 3 101944711 intron variant A/G;T snv 2
rs12489120 1.000 0.040 3 4978778 intron variant C/A;G;T snv 1
rs4845454 0.925 0.040 1 152619708 downstream gene variant C/A;T snv 1
rs367569 0.807 0.120 16 11271643 intron variant C/T snv 0.32 6
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 5
rs33980500 0.742 0.200 6 111592059 missense variant C/T snv 8.6E-02 9.7E-02 3
rs1056198 0.925 0.040 20 49939692 intron variant C/T snv 0.34 2
rs2066819 0.925 0.040 12 56356420 intron variant C/T snv 4.9E-02 4.5E-02 2
rs11652075 0.882 0.040 17 80205094 missense variant C/T snv 0.41 0.40 1
rs2675669 1.000 0.040 10 73894114 intergenic variant C/T snv 0.55 1
rs6474412 0.925 0.120 8 42695355 upstream gene variant C/T snv 0.64 1
rs28998802 0.807 0.120 17 27797882 intron variant G/A snv 0.11 6
rs1250544 0.882 0.080 10 79273128 intron variant G/A snv 0.32 3
rs17728338 0.851 0.160 5 151098757 downstream gene variant G/A snv 7.1E-02 2