Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs855791 0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 17
rs4246905 0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 15
rs62324212 0.724 0.240 4 122639784 intron variant C/A;G snv 15
rs10988542 0.724 0.240 9 129894985 intron variant G/A;C snv 14
rs11145763 0.724 0.240 9 136369144 intron variant A/C;G;T snv 14
rs11580078 0.724 0.240 1 67203951 intron variant C/A;G snv 14
rs1332099 0.724 0.240 10 99538694 downstream gene variant T/C;G snv 14
rs2738774 0.724 0.240 20 63637985 downstream gene variant G/A;C snv 14
rs2807264 0.724 0.240 X 136583619 downstream gene variant C/A snv 14
rs4869313 0.724 0.240 5 96888176 intron variant T/A;G snv 14
rs55705316 0.724 0.240 1 206760172 regulatory region variant T/A;G snv 14
rs7660520 0.724 0.240 4 182824168 upstream gene variant G/A;C snv 14
rs7831697 0.724 0.240 8 137124061 regulatory region variant T/A;C;G snv 14
rs11221332 0.763 0.280 11 128511079 intron variant C/A;T snv 8
rs1893592 0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 7
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs17849502 0.827 0.240 1 183563445 missense variant G/A;C;T snv 4.0E-06; 4.0E-06; 3.4E-02 5
rs7579944 0.882 0.200 2 30222160 intergenic variant T/C;G snv 5
rs9979383 0.925 0.200 21 35343463 intron variant C/G;T snv 5
rs802734 0.827 0.280 6 127957653 intergenic variant A/G;T snv 4
rs11066188 0.851 0.320 12 112172910 intron variant G/A;C snv 0.30; 4.1E-06 3
rs212388 0.827 0.240 6 159069404 intron variant C/G;T snv 3
rs10188217 0.925 0.080 2 60990407 intron variant T/A;C snv 2
rs12734338 0.925 0.120 1 202500595 intron variant T/C snv 2