Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1056198 0.925 0.040 20 49939692 intron variant C/T snv 0.34 2
rs10865331 0.827 0.120 2 62324337 intergenic variant A/G snv 0.57 5
rs11652075 0.882 0.040 17 80205094 missense variant C/T snv 0.41 0.40 1
rs12445568 0.925 0.040 16 30993491 splice region variant T/C snv 0.39 0.38 2
rs12489120 1.000 0.040 3 4978778 intron variant C/A;G;T snv 1
rs1250544 0.882 0.080 10 79273128 intron variant G/A snv 0.32 3
rs12884468 0.925 0.040 14 35383280 downstream gene variant T/C snv 0.47 2
rs1295685 0.790 0.160 5 132660753 3 prime UTR variant A/G snv 0.81 4
rs17716942 0.925 0.040 2 162404181 intron variant T/C snv 9.6E-02 2
rs17728338 0.851 0.160 5 151098757 downstream gene variant G/A snv 7.1E-02 2
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 2
rs181359 0.882 0.080 22 21574352 intron variant G/A snv 0.21 2
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 4
rs2066819 0.925 0.040 12 56356420 intron variant C/T snv 4.9E-02 4.5E-02 2
rs2233278 0.925 0.040 5 151087628 5 prime UTR variant G/C;T snv 4.8E-02 2
rs2395029 0.790 0.320 6 31464003 non coding transcript exon variant T/G snv 2.7E-02 2.4E-02 7
rs2675662 0.925 0.040 10 73839369 intron variant A/G snv 0.55 2
rs2675669 1.000 0.040 10 73894114 intergenic variant C/T snv 0.55 1
rs27432 0.925 0.040 5 96783569 intron variant A/C;G snv 2
rs27524 0.851 0.160 5 96766240 intron variant A/G snv 0.61 1
rs28998802 0.807 0.120 17 27797882 intron variant G/A snv 0.11 6
rs30187 0.732 0.360 5 96788627 missense variant T/A;C snv 0.62 1
rs3135388 0.807 0.240 6 32445274 downstream gene variant A/G snv 0.90 1
rs33980500 0.742 0.200 6 111592059 missense variant C/T snv 8.6E-02 9.7E-02 3
rs34536443 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 20