Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1004467 | 0.790 | 0.280 | 10 | 102834750 | non coding transcript exon variant | A/G | snv | 0.15 | 0.14 | 13 | |
rs10059884 | 5 | 32832368 | regulatory region variant | C/A;T | snv | 5 | |||||
rs10184428 | 2 | 164155317 | intron variant | C/A;G | snv | 5 | |||||
rs10255839 | 7 | 27249498 | intron variant | G/A | snv | 0.87 | 6 | ||||
rs10504249 | 8 | 57876522 | intron variant | A/G | snv | 1.7E-02 | 3 | ||||
rs10776752 | 1 | 112501706 | intron variant | G/T | snv | 8.8E-02 | 4 | ||||
rs10857147 | 1.000 | 0.040 | 4 | 80259918 | intergenic variant | A/T | snv | 0.25 | 9 | ||
rs10897164 | 11 | 61510303 | 3 prime UTR variant | A/G | snv | 0.13 | 3 | ||||
rs10930597 | 2 | 173462117 | intergenic variant | C/T | snv | 0.14 | 3 | ||||
rs10948071 | 6 | 43312975 | intron variant | C/T | snv | 0.46 | 4 | ||||
rs11014166 | 0.882 | 0.040 | 10 | 18419869 | intron variant | A/T | snv | 0.27 | 10 | ||
rs11024074 | 0.925 | 0.040 | 11 | 16895672 | intron variant | T/C | snv | 0.29 | 5 | ||
rs1105955 | 6 | 126826023 | intron variant | T/A | snv | 0.44 | 3 | ||||
rs1105956 | 6 | 126825734 | intron variant | G/A | snv | 0.44 | 2 | ||||
rs11065979 | 0.851 | 0.200 | 12 | 111621753 | intergenic variant | C/T | snv | 0.30 | 12 | ||
rs11099097 | 4 | 80246155 | intergenic variant | C/T | snv | 0.30 | 6 | ||||
rs11099098 | 0.925 | 0.120 | 4 | 80248758 | intergenic variant | G/C;T | snv | 8 | |||
rs11105352 | 12 | 89632685 | intron variant | G/A | snv | 0.14 | 4 | ||||
rs11105364 | 12 | 89675499 | intron variant | T/G | snv | 0.15 | 4 | ||||
rs111478946 | 12 | 89665065 | intron variant | G/A | snv | 0.14 | 4 | ||||
rs11191548 | 0.882 | 0.080 | 10 | 103086421 | 3 prime UTR variant | T/C | snv | 8.6E-02 | 10 | ||
rs11191871 | 10 | 103947673 | intergenic variant | A/G | snv | 5.2E-02 | 2 | ||||
rs112640876 | 11 | 1873813 | intron variant | A/G;T | snv | 3 | |||||
rs112862634 | 5 | 88674534 | intron variant | G/C | snv | 0.17 | 3 | ||||
rs11513729 | 1.000 | 0.080 | 12 | 111835695 | downstream gene variant | C/T | snv | 0.29 | 5 |