Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10035291 | 1.000 | 0.040 | 5 | 81500549 | intron variant | T/C | snv | 0.46 | 1 | ||
rs10058613 | 0.925 | 0.040 | 5 | 138358306 | intron variant | C/A;G;T | snv | 2 | |||
rs1006737 | 0.695 | 0.120 | 12 | 2236129 | intron variant | G/A | snv | 0.36 | 7 | ||
rs1012053 | 1.000 | 0.040 | 13 | 42079301 | intron variant | C/A | snv | 0.85 | 1 | ||
rs10134944 | 1.000 | 0.040 | 14 | 57652478 | intron variant | C/T | snv | 0.13 | 1 | ||
rs10168049 | 1.000 | 0.040 | 2 | 121320830 | intergenic variant | A/G | snv | 0.16 | 1 | ||
rs10198175 | 0.925 | 0.080 | 2 | 20934123 | intergenic variant | A/G | snv | 0.93 | 3 | ||
rs10275045 | 0.882 | 0.160 | 7 | 1881190 | intron variant | C/T | snv | 0.35 | 5 | ||
rs1039002 | 0.851 | 0.080 | 6 | 165741969 | intron variant | G/A;T | snv | 1 | |||
rs10405744 | 0.851 | 0.040 | 19 | 19948684 | intron variant | G/A | snv | 9.0E-02 | 4 | ||
rs1042779 | 0.882 | 0.040 | 3 | 52786995 | missense variant | A/G | snv | 0.40 | 0.42 | 3 | |
rs10455979 | 1.000 | 0.040 | 6 | 166581772 | intron variant | C/A;G;T | snv | 1 | |||
rs10457441 | 1.000 | 0.040 | 6 | 98124244 | intron variant | T/A;C | snv | 2 | |||
rs10459221 | 1.000 | 0.040 | 12 | 49073211 | upstream gene variant | C/A;G | snv | 1 | |||
rs10488140 | 1.000 | 0.040 | 7 | 55070695 | intron variant | C/T | snv | 0.26 | 1 | ||
rs10489167 | 1.000 | 0.040 | 1 | 40710794 | intron variant | G/A | snv | 0.13 | 1 | ||
rs10489744 | 0.925 | 0.040 | 1 | 165411386 | intron variant | G/A | snv | 0.55 | 2 | ||
rs10501439 | 1.000 | 0.040 | 11 | 79374802 | intron variant | A/G | snv | 0.18 | 1 | ||
rs10503253 | 0.851 | 0.040 | 8 | 4323322 | intron variant | C/A | snv | 0.18 | 5 | ||
rs10509129 | 1.000 | 0.040 | 10 | 60311283 | intron variant | G/A;T | snv | 1 | |||
rs10511083 | 1.000 | 0.040 | 3 | 85521809 | intron variant | A/G | snv | 0.51 | 1 | ||
rs10512928 | 1.000 | 0.040 | 5 | 7546298 | intron variant | C/T | snv | 0.15 | 1 | ||
rs10513249 | 1.000 | 0.040 | 9 | 114541631 | intergenic variant | C/A;G | snv | 1 | |||
rs1054442 | 0.925 | 0.040 | 12 | 48995537 | 3 prime UTR variant | A/C | snv | 0.46 | 4 | ||
rs105633 | 0.882 | 0.040 | 5 | 141945684 | synonymous variant | T/C;G | snv | 0.98; 4.0E-06 | 3 |