Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12696304 | 0.776 | 0.320 | 3 | 169763483 | downstream gene variant | C/G | snv | 0.38 | 10 | ||
rs380286 | 0.776 | 0.200 | 5 | 1320132 | intron variant | G/A | snv | 0.47 | 8 | ||
rs35158985 | 0.882 | 0.080 | 16 | 68762843 | intron variant | A/G | snv | 0.38 | 6 | ||
rs4778138 | 0.851 | 0.080 | 15 | 28090674 | intron variant | A/G;T | snv | 6 | |||
rs10739221 | 0.851 | 0.080 | 9 | 106298549 | intron variant | T/C;G | snv | 5 | |||
rs132985 | 0.827 | 0.120 | 22 | 38167464 | intron variant | C/T | snv | 0.51 | 5 | ||
rs251464 | 0.851 | 0.080 | 5 | 149816671 | intron variant | G/C | snv | 0.36 | 5 | ||
rs10816595 | 0.851 | 0.080 | 9 | 107947454 | regulatory region variant | A/G | snv | 0.33 | 4 | ||
rs498136 | 0.851 | 0.080 | 11 | 69552350 | intergenic variant | A/C | snv | 0.68 | 4 | ||
rs1636744 | 0.851 | 0.080 | 7 | 16944656 | intron variant | C/T | snv | 0.31 | 4 | ||
rs6914598 | 0.851 | 0.080 | 6 | 21163688 | intron variant | T/C | snv | 0.38 | 4 | ||
rs75570604 | 0.851 | 0.080 | 16 | 89780269 | intron variant | G/C | snv | 4.7E-02 | 4 | ||
rs869329 | 0.851 | 0.080 | 9 | 21804694 | intron variant | A/G;T | snv | 4 | |||
rs34466956 | 0.882 | 0.080 | 19 | 3353624 | intron variant | C/T | snv | 0.49 | 4 | ||
rs56238684 | 0.882 | 0.080 | 20 | 34648892 | intron variant | G/C | snv | 4.2E-02 | 4 | ||
rs6750047 | 0.851 | 0.080 | 2 | 38049406 | intron variant | A/G | snv | 0.61 | 4 | ||
rs2995264 | 0.851 | 0.080 | 10 | 103909085 | intron variant | G/A | snv | 0.88 | 4 | ||
rs10830253 | 0.851 | 0.080 | 11 | 89294875 | intron variant | T/G | snv | 0.29 | 4 | ||
rs2111398 | 0.882 | 0.080 | 12 | 12922268 | downstream gene variant | A/G | snv | 0.49 | 3 | ||
rs2695237 | 0.882 | 0.080 | 1 | 226415934 | upstream gene variant | T/A;C | snv | 3 | |||
rs7041168 | 0.882 | 0.080 | 9 | 107936435 | intergenic variant | G/A;T | snv | 3 | |||
rs75691080 | 0.882 | 0.080 | 20 | 63638397 | downstream gene variant | C/T | snv | 9.1E-02 | 3 | ||
rs72704658 | 0.882 | 0.080 | 1 | 150860534 | intron variant | T/C | snv | 0.33 | 3 | ||
rs73008229 | 0.882 | 0.080 | 11 | 108316962 | intron variant | G/A | snv | 0.11 | 3 | ||
rs4670813 | 0.882 | 0.080 | 2 | 38090568 | intron variant | G/A | snv | 0.40 | 3 |