Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7552167 0.807 0.120 1 24192153 upstream gene variant A/G snv 0.87 6
rs9988642 0.882 0.080 1 67260421 downstream gene variant T/C snv 0.13 3
rs7536201 0.925 0.040 1 24966593 upstream gene variant T/C;G snv 2
rs4649203 0.851 0.160 1 24193430 intergenic variant G/A snv 0.61 1
rs4845454 0.925 0.040 1 152619708 downstream gene variant C/A;T snv 1
rs10865331 0.827 0.120 2 62324337 intergenic variant A/G snv 0.57 5
rs17716942 0.925 0.040 2 162404181 intron variant T/C snv 9.6E-02 2
rs62149416 0.925 0.040 2 60856371 intron variant T/C snv 0.26 2
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 2
rs4683946 0.925 0.080 3 101896982 intron variant G/T snv 0.19 2
rs4685408 0.925 0.040 3 16954543 intron variant G/A snv 0.56 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
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
rs17728338 0.851 0.160 5 151098757 downstream gene variant G/A snv 7.1E-02 2
rs2233278 0.925 0.040 5 151087628 5 prime UTR variant G/C;T snv 4.8E-02 2
rs27432 0.925 0.040 5 96783569 intron variant A/C;G snv 2
rs7709212 0.925 0.040 5 159337169 intron variant T/C snv 0.34 2
rs27524 0.851 0.160 5 96766240 intron variant A/G snv 0.61 1
rs30187 0.732 0.360 5 96788627 missense variant T/A;C snv 0.62 1
rs2395029 0.790 0.320 6 31464003 non coding transcript exon variant T/G snv 2.7E-02 2.4E-02 7
rs9264942 0.763 0.400 6 31306603 intron variant T/C snv 0.34 5
rs33980500 0.742 0.200 6 111592059 missense variant C/T snv 8.6E-02 9.7E-02 3
rs4406273 0.925 0.040 6 31298313 intron variant G/A snv 8.6E-02 2