Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs201921722 | 0.925 | 0.040 | 11 | 123679999 | downstream gene variant | -/A | delins | 9.2E-06 | 3 | ||
rs58598658 | 0.925 | 0.080 | 13 | 73887725 | intron variant | -/A;AA | delins | 4 | |||
rs1799752 | 0.677 | 0.480 | 17 | 63488529 | intron variant | -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT | delins | 25 | |||
rs34177316 | 0.925 | 0.040 | 4 | 40985283 | intron variant | A/-;AA;AAA | delins | 3 | |||
rs528732638 | 0.851 | 0.120 | 18 | 26940224 | intron variant | A/-;AA;AAA;AAAA | delins | 5 | |||
rs1333048 | 0.683 | 0.320 | 9 | 22125348 | intron variant | A/C | snv | 0.44 | 24 | ||
rs1176744 | 0.708 | 0.240 | 11 | 113932306 | missense variant | A/C | snv | 0.33 | 0.36 | 19 | |
rs8321 | 0.742 | 0.320 | 6 | 30064745 | 3 prime UTR variant | A/C | snv | 5.4E-02 | 5.9E-02 | 16 | |
rs242941 | 0.790 | 0.200 | 17 | 45815154 | intron variant | A/C | snv | 0.62 | 9 | ||
rs11568817 | 0.790 | 0.120 | 6 | 77463665 | 5 prime UTR variant | A/C | snv | 0.37 | 8 | ||
rs2522833 | 0.827 | 0.080 | 7 | 82824392 | missense variant | A/C | snv | 0.45 | 0.34 | 7 | |
rs2619522 | 0.827 | 0.080 | 6 | 15653418 | intron variant | A/C | snv | 0.26 | 6 | ||
rs11152369 | 0.851 | 0.040 | 18 | 55399097 | intron variant | A/C | snv | 6.3E-02 | 5 | ||
rs7296288 | 0.851 | 0.080 | 12 | 49086185 | upstream gene variant | A/C | snv | 0.50 | 5 | ||
rs17673138 | 0.851 | 0.040 | 8 | 32840440 | intron variant | A/C | snv | 8.6E-02 | 4 | ||
rs2709370 | 0.851 | 0.120 | 2 | 207517878 | intron variant | A/C | snv | 0.17 | 4 | ||
rs2546057 | 1.000 | 0.040 | 19 | 33829949 | intergenic variant | A/C | snv | 0.41 | 3 | ||
rs11039409 | 1.000 | 0.040 | 11 | 47814169 | intron variant | A/C | snv | 0.22 | 2 | ||
rs16854048 | 1.000 | 0.040 | 4 | 42121711 | intron variant | A/C | snv | 0.23 | 2 | ||
rs184924771 | 1.000 | 0.040 | 11 | 25863658 | intergenic variant | A/C | snv | 1.2E-02 | 2 | ||
rs2073380 | 0.925 | 0.040 | 21 | 46443844 | missense variant | A/C | snv | 0.22 | 0.18 | 2 | |
rs2286798 | 1.000 | 0.040 | 3 | 52787161 | intron variant | A/C | snv | 0.38 | 0.37 | 2 | |
rs56403421 | 1.000 | 0.040 | 18 | 55098052 | regulatory region variant | A/C | snv | 0.26 | 2 | ||
rs600011 | 1.000 | 0.040 | 3 | 107576545 | intron variant | A/C | snv | 0.25 | 2 | ||
rs72788286 | 1.000 | 0.040 | 2 | 23875451 | intron variant | A/C | snv | 0.12 | 2 |