Source: GWASCAT ×
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11145763 | 0.724 | 0.240 | 9 | 136369144 | intron variant | A/C;G;T | snv | 14 | |||
rs12598357 | 0.724 | 0.240 | 16 | 28329624 | intergenic variant | A/G | snv | 0.43 | 15 | ||
rs1270942 | 0.742 | 0.440 | 6 | 31951083 | non coding transcript exon variant | A/G | snv | 7.5E-02 | 3 | ||
rs17466626 | 0.724 | 0.240 | 12 | 40366829 | non coding transcript exon variant | A/G | snv | 1.7E-02 | 14 | ||
rs2111485 | 0.724 | 0.280 | 2 | 162254026 | regulatory region variant | A/G | snv | 0.46 | 12 | ||
rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 34 | |
rs4625 | 0.716 | 0.280 | 3 | 49534707 | 3 prime UTR variant | A/G | snv | 0.30 | 17 | ||
rs72743477 | 0.724 | 0.240 | 15 | 67171953 | intron variant | A/G | snv | 0.17 | 14 | ||
rs2304256 | 0.732 | 0.360 | 19 | 10364976 | missense variant | C/A | snv | 0.27 | 0.23 | 3 | |
rs2807264 | 0.724 | 0.240 | X | 136583619 | downstream gene variant | C/A | snv | 14 | |||
rs6679677 | 0.653 | 0.320 | 1 | 113761186 | upstream gene variant | C/A | snv | 6.7E-02 | 25 | ||
rs11580078 | 0.724 | 0.240 | 1 | 67203951 | intron variant | C/A;G | snv | 14 | |||
rs62324212 | 0.724 | 0.240 | 4 | 122639784 | intron variant | C/A;G | snv | 15 | |||
rs12863738 | 0.724 | 0.240 | X | 136949968 | intron variant | C/T | snv | 0.16 | 14 | ||
rs17885785 | 0.724 | 0.240 | 11 | 2146620 | non coding transcript exon variant | C/T | snv | 0.14 | 14 | ||
rs1990760 | 0.672 | 0.480 | 2 | 162267541 | missense variant | C/T | snv | 0.50 | 0.45 | 7 | |
rs2066363 | 0.724 | 0.240 | 1 | 81771892 | intron variant | C/T | snv | 0.71 | 14 | ||
rs34884278 | 0.724 | 0.240 | 1 | 172869708 | intron variant | C/T | snv | 0.63 | 14 | ||
rs36001488 | 0.724 | 0.240 | 2 | 233276621 | intron variant | C/T | snv | 0.44 | 14 | ||
rs62131887 | 0.724 | 0.240 | 19 | 10476920 | intergenic variant | C/T | snv | 0.37 | 14 | ||
rs653178 | 0.672 | 0.600 | 12 | 111569952 | intron variant | C/T | snv | 0.67 | 23 | ||
rs706778 | 0.695 | 0.320 | 10 | 6056986 | intron variant | C/T | snv | 0.46 | 15 | ||
rs755374 | 0.724 | 0.240 | 5 | 159402286 | intron variant | C/T | snv | 0.28 | 14 | ||
rs77150043 | 0.724 | 0.240 | 16 | 50270338 | intron variant | C/T | snv | 0.17 | 14 | ||
rs7725052 | 0.716 | 0.240 | 5 | 40487168 | intron variant | C/T | snv | 0.52 | 15 |