Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs306890
SPRY3
Y 56944005 intergenic variant T/C snv 4
rs4129148 1.000 0.040 Y 1029445 intergenic variant C/G;T snv 1
rs12863738 0.724 0.240 X 136949968 intron variant C/T snv 0.16 14
rs2807264 0.724 0.240 X 136583619 downstream gene variant C/A snv 14
rs5934683
GPR143
0.790 0.080 X 9783434 intron variant T/C snv 0.50 9
rs2732875
SHROOM2
0.790 0.080 X 9795858 intron variant C/G;T snv 9
rs5934505 0.776 0.120 X 8945785 intergenic variant T/A;C snv 8
rs55846652 0.776 0.160 X 69564858 downstream gene variant T/C snv 0.29 8
rs2497938 0.807 0.080 X 67343176 intergenic variant T/C snv 0.37 7
rs6625163 0.807 0.080 X 67291142 intergenic variant G/A snv 0.62 7
rs7061504
OPHN1
0.807 0.080 X 68143959 intron variant A/G snv 0.23 7
rs1050828
G6PD
0.790 0.200 X 154536002 missense variant C/T snv 9.1E-03 3.6E-02 6
rs5933688 0.827 0.080 X 8912639 intron variant A/G snv 0.24 6
rs200644307 0.827 0.080 X 67081072 intergenic variant -/CATAAATATGTGTATATATA;CATAAATATGTGTATATATGTGTATATATACATAAATATGTGTATATATA delins 6
rs143149578
KLF8
0.827 0.080 X 55923583 intron variant C/T snv 4.3E-04 6
rs111763724 0.827 0.080 X 57975900 intergenic variant A/G snv 7.8E-02 6
rs185597083 0.827 0.080 X 55107412 intergenic variant C/A snv 2.1E-02 6
rs7890572
IL1RAPL1
X 29622701 intron variant A/G snv 9.3E-02 5
rs114209171
FUNDC2
0.882 0.120 X 155050522 non coding transcript exon variant T/C snv 0.23 5
rs6637197 1.000 X 144281548 intergenic variant C/A;G;T snv 5
rs5985471 X 110460733 downstream gene variant C/T snv 0.43 4
rs5942937 X 110473179 intron variant T/G snv 0.47 4
rs17324272 1.000 X 133003128 intergenic variant T/C snv 3.2E-03 4
rs762516
G6PD
X 154536448 intron variant C/T snv 4.7E-02 3
rs190783615 0.925 0.040 X 142772620 intergenic variant T/C snv 9.3E-03 3