Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs452159 | 1.000 | 0.040 | 20 | 44642461 | intron variant | G/T | snv | 0.28 | 2 | ||
rs4822489 | 0.925 | 0.200 | 22 | 24437792 | intron variant | T/G | snv | 0.48 | 2 | ||
rs6684209 | 1.000 | 0.040 | 1 | 115707991 | intron variant | C/T | snv | 0.17 | 2 | ||
rs6787362 | 0.925 | 0.040 | 3 | 69178228 | intron variant | A/G | snv | 9.3E-02 | 2 | ||
rs9303504 | 0.925 | 0.040 | 17 | 66319248 | intron variant | G/C | snv | 0.59 | 2 | ||
rs9909004 | 0.925 | 0.040 | 17 | 66310015 | intron variant | C/T | snv | 0.59 | 2 | ||
rs1009388 | 1.000 | 0.040 | 2 | 25168232 | intron variant | G/C | snv | 0.18 | 1 | ||
rs1544223 | 1.000 | 0.040 | 1 | 111503935 | intron variant | C/T | snv | 0.72 | 1 | ||
rs28714259 | 0.882 | 0.120 | 15 | 23463380 | intergenic variant | G/A | snv | 0.19 | 5 | ||
rs10189761 | 0.882 | 0.120 | 2 | 646364 | intergenic variant | T/A | snv | 0.82 | 4 | ||
rs9351814 | 0.882 | 0.040 | 6 | 71484004 | intergenic variant | A/C | snv | 0.35 | 4 | ||
rs9885413 | 0.925 | 0.040 | 5 | 110840429 | intergenic variant | G/T | snv | 0.19 | 2 | ||
rs73956431 | 0.827 | 0.120 | 18 | 31699870 | regulatory region variant | C/T | snv | 8.4E-02 | 6 | ||
rs1042714 | 0.597 | 0.640 | 5 | 148826910 | stop gained | G/C;T | snv | 0.68 | 54 | ||
rs5219 | 0.701 | 0.360 | 11 | 17388025 | stop gained | T/A;C | snv | 0.64 | 25 | ||
rs1815739 | 0.763 | 0.240 | 11 | 66560624 | stop gained | C/T | snv | 0.37 | 17 | ||
rs766265889 | 0.827 | 0.240 | 2 | 178535508 | stop gained | G/A;T | snv | 8.0E-06; 4.0E-06 | 11 | ||
rs111033560 | 0.807 | 0.040 | 6 | 118559037 | stop gained | T/G | snv | 1.6E-05 | 9 | ||
rs767312316 | 1.000 | 0.040 | 17 | 82375046 | stop gained | C/A;G;T | snv | 6.6E-05; 1.7E-05; 1.7E-05 | 1 | ||
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs1799983 | 0.430 | 0.880 | 7 | 150999023 | missense variant | T/A;G | snv | 0.75 | 246 | ||
rs1799945 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 226 | |
rs1695 | 0.457 | 0.880 | 11 | 67585218 | missense variant | A/G | snv | 0.34 | 0.36 | 188 | |
rs699 | 0.501 | 0.800 | 1 | 230710048 | missense variant | A/G | snv | 0.55 | 0.58 | 134 | |
rs1801282 | 0.500 | 0.840 | 3 | 12351626 | missense variant | C/G | snv | 0.11 | 8.9E-02 | 131 |