Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12210050 | 0.807 | 0.040 | 6 | 475489 | non coding transcript exon variant | C/T | snv | 0.11 | 8 | ||
rs7335046 | 0.807 | 0.040 | 13 | 99389484 | downstream gene variant | G/C | snv | 0.80 | 7 | ||
rs1246946 | 0.851 | 0.040 | 6 | 4979722 | downstream gene variant | C/T | snv | 0.34 | 4 | ||
rs4761496 | 0.851 | 0.040 | 12 | 94733833 | regulatory region variant | T/A;C | snv | 0.23 | 4 | ||
rs7297245 | 0.882 | 0.040 | 12 | 95980836 | missense variant | C/T | snv | 0.85 | 0.86 | 4 | |
rs75790006 | 0.851 | 0.040 | 4 | 43211547 | intron variant | T/G | snv | 1.1E-02 | 4 | ||
rs2847281 | 1.000 | 0.040 | 18 | 12821594 | intron variant | A/G | snv | 0.32 | 3 | ||
rs7309332 | 1.000 | 0.040 | 12 | 7938243 | upstream gene variant | T/C | snv | 0.59 | 3 | ||
rs74664507 | 1.000 | 0.040 | 9 | 16913838 | upstream gene variant | T/A | snv | 3 | |||
rs1047325 | 1.000 | 0.040 | 1 | 153561551 | missense variant | C/T | snv | 7.1E-02 | 0.16 | 2 | |
rs10759637 | 1.000 | 0.040 | 9 | 113262744 | 3 prime UTR variant | A/C | snv | 0.47 | 2 | ||
rs121913082 | 1.000 | 0.040 | 10 | 89014205 | missense variant | A/G | snv | 2 | |||
rs121913083 | 1.000 | 0.040 | 10 | 89008907 | missense variant | A/G | snv | 2 | |||
rs121913084 | 1.000 | 0.040 | 10 | 89010779 | missense variant | T/C | snv | 2 | |||
rs1670661 | 1.000 | 0.040 | 11 | 21209124 | intron variant | C/G;T | snv | 2 | |||
rs17761864 | 1.000 | 0.040 | 17 | 2268343 | intron variant | C/A | snv | 0.28 | 2 | ||
rs2239612 | 1.000 | 0.040 | 3 | 187075454 | intron variant | G/A | snv | 0.17 | 2 | ||
rs4785204 | 1.000 | 0.040 | 16 | 50069823 | intron variant | C/T | snv | 8.6E-02 | 2 | ||
rs6413464 | 1.000 | 0.040 | 9 | 21970980 | missense variant | C/A;G | snv | 1.3E-03; 4.1E-06 | 2 | ||
rs6503659 | 1.000 | 0.040 | 17 | 41741012 | intergenic variant | A/C;G;T | snv | 2 | |||
rs1064793400 | 1.000 | 0.040 | 3 | 37048550 | missense variant | G/A | snv | 1 | |||
rs1064793981 | 1.000 | 0.040 | 2 | 47475030 | missense variant | G/A | snv | 1 | |||
rs1078305 | 1.000 | 0.040 | 9 | 121289122 | intron variant | A/G | snv | 0.70 | 1 | ||
rs10818524 | 1.000 | 0.040 | 9 | 121267901 | intron variant | T/C | snv | 0.37 | 1 | ||
rs10971638 | 1.000 | 0.040 | 9 | 33674679 | non coding transcript exon variant | C/T | snv | 0.21 | 1 |