Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1056513 | 1 | 61914626 | missense variant | G/A;C | snv | 0.57; 8.0E-06 | 3 | ||||
rs7498665 | 0.925 | 0.120 | 16 | 28871920 | missense variant | A/G;T | snv | 0.35 | 9 | ||
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 272 | |
rs8050136 | 0.716 | 0.560 | 16 | 53782363 | intron variant | C/A | snv | 0.40 | 32 | ||
rs1558902 | 0.827 | 0.120 | 16 | 53769662 | intron variant | T/A | snv | 0.31 | 21 | ||
rs143384 | 0.827 | 0.200 | 20 | 35437976 | 5 prime UTR variant | G/A | snv | 0.44 | 17 | ||
rs7138803 | 0.827 | 0.240 | 12 | 49853685 | intergenic variant | G/A;T | snv | 17 | |||
rs9930506 | 0.776 | 0.360 | 16 | 53796553 | intron variant | A/G | snv | 0.36 | 16 | ||
rs12970134 | 0.790 | 0.280 | 18 | 60217517 | intergenic variant | G/A | snv | 0.21 | 13 | ||
rs925946 | 0.882 | 0.120 | 11 | 27645655 | intron variant | T/G | snv | 0.72 | 9 | ||
rs12967135 | 18 | 60181790 | intergenic variant | G/A | snv | 0.24 | 8 | ||||
rs2568958 | 0.882 | 0.160 | 1 | 72299433 | intron variant | G/A;C | snv | 8 | |||
rs7647305 | 1.000 | 0.080 | 3 | 186116501 | intron variant | T/C | snv | 0.74 | 8 | ||
rs10913469 | 1.000 | 0.080 | 1 | 177944384 | intron variant | T/C | snv | 0.22 | 7 | ||
rs2531995 | 1.000 | 0.080 | 16 | 3963466 | 3 prime UTR variant | C/T | snv | 0.45 | 7 | ||
rs6499640 | 0.925 | 0.160 | 16 | 53735765 | intron variant | G/A | snv | 0.59 | 7 | ||
rs7531118 | 1.000 | 0.080 | 1 | 72371556 | intron variant | T/C | snv | 0.40 | 7 | ||
rs7561317 | 0.925 | 0.120 | 2 | 644953 | intergenic variant | A/G | snv | 0.81 | 7 | ||
rs29941 | 1.000 | 0.080 | 19 | 33818627 | downstream gene variant | A/G | snv | 0.70 | 6 | ||
rs113191842 | 16 | 53783406 | intron variant | G/A | snv | 9.4E-02 | 5 | ||||
rs11847697 | 14 | 30045906 | intron variant | C/T | snv | 0.13 | 5 | ||||
rs2844479 | 0.925 | 0.200 | 6 | 31605179 | intergenic variant | A/C | snv | 0.34 | 5 | ||
rs177430 | 18 | 23506161 | intron variant | C/A;T | snv | 4 | |||||
rs9813495 | 3 | 85777231 | intron variant | A/G | snv | 0.15 | 4 | ||||
rs11863065 | 16 | 82293200 | intergenic variant | G/A | snv | 7.3E-02 | 3 |