Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11605020 | 1.000 | 0.040 | 11 | 127110970 | intron variant | G/A;C | snv | 2 | |||
rs11608355 | 1.000 | 0.040 | 12 | 109441487 | intron variant | T/C | snv | 0.33 | 2 | ||
rs116362708 | 1.000 | 0.040 | 1 | 75464629 | intron variant | G/A | snv | 2.3E-02 | 2 | ||
rs11663393 | 1.000 | 0.040 | 18 | 53088362 | intron variant | G/A | snv | 0.40 | 2 | ||
rs11664123 | 1.000 | 0.040 | 18 | 53440658 | intron variant | T/C | snv | 0.24 | 2 | ||
rs11693031 | 1.000 | 0.040 | 2 | 211813206 | intron variant | A/G;T | snv | 2 | |||
rs117198528 | 1.000 | 0.040 | 18 | 49694188 | intergenic variant | T/G | snv | 1.0E-02 | 3 | ||
rs11826064 | 1.000 | 0.040 | 11 | 50818695 | intergenic variant | C/A;T | snv | 2 | |||
rs11924809 | 0.925 | 0.040 | 3 | 186353656 | intron variant | G/A | snv | 5.3E-02 | 3 | ||
rs12030991 | 1.000 | 0.040 | 1 | 106683737 | intergenic variant | G/C;T | snv | 2 | |||
rs12068879 | 1.000 | 0.040 | 1 | 14959860 | intron variant | A/G | snv | 0.18 | 2 | ||
rs12137398 | 1.000 | 0.040 | 1 | 7730488 | intron variant | C/T | snv | 0.14 | 2 | ||
rs12137936 | 1.000 | 0.040 | 1 | 72254674 | intron variant | C/G | snv | 0.23 | 2 | ||
rs12420205 | 1.000 | 0.040 | 11 | 113523313 | intergenic variant | C/T | snv | 0.65 | 2 | ||
rs12457157 | 1.000 | 0.040 | 18 | 55629696 | intron variant | G/A | snv | 0.41 | 2 | ||
rs1261070 | 1.000 | 0.040 | 18 | 55235854 | intron variant | A/G | snv | 0.94 | 2 | ||
rs1261114 | 1.000 | 0.040 | 18 | 55271138 | intron variant | G/A | snv | 0.46 | 2 | ||
rs12938031 | 0.851 | 0.160 | 17 | 45777136 | intron variant | A/G | snv | 0.26 | 4 | ||
rs12938775 | 1.000 | 0.040 | 17 | 2671527 | intron variant | G/A;T | snv | 2 | |||
rs12963463 | 1.000 | 0.040 | 18 | 55431862 | intron variant | C/G;T | snv | 3 | |||
rs12967855 | 1.000 | 0.040 | 18 | 37558282 | intron variant | A/G | snv | 0.52 | 2 | ||
rs13060816 | 1.000 | 0.040 | 3 | 107561639 | intron variant | T/A;C | snv | 2 | |||
rs13122395 | 1.000 | 0.040 | 4 | 100829496 | intron variant | G/A | snv | 0.34 | 2 | ||
rs1322281 | 1.000 | 0.040 | 9 | 10582445 | intron variant | T/C | snv | 0.76 | 2 | ||
rs13296664 | 1.000 | 0.040 | 9 | 117684418 | downstream gene variant | C/T | snv | 0.22 | 2 |