Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1021479 | 16 | 85923808 | upstream gene variant | T/A;C | snv | 2 | |||||
rs10276619 | 1.000 | 0.080 | 7 | 50273756 | downstream gene variant | G/A | snv | 0.59 | 2 | ||
rs10489481 | 1 | 185422035 | regulatory region variant | G/A | snv | 0.31 | 2 | ||||
rs10987830 | 9 | 128016459 | intergenic variant | G/A | snv | 6.8E-03 | 2 | ||||
rs112313229 | 3 | 46323369 | intergenic variant | G/A;T | snv | 2 | |||||
rs112721625 | 17 | 59850066 | upstream gene variant | TT/-;T;TTT;TTTT | delins | 2 | |||||
rs11640143 | 16 | 85955858 | regulatory region variant | T/C;G | snv | 2 | |||||
rs11686139 | 2 | 226426699 | intergenic variant | A/C | snv | 0.13 | 2 | ||||
rs117424492 | 15 | 79975053 | upstream gene variant | G/C;T | snv | 2 | |||||
rs11775706 | 8 | 6843366 | intron variant | C/G;T | snv | 2 | |||||
rs11992162 | 8 | 11979005 | upstream gene variant | G/A;C;T | snv | 2 | |||||
rs12149363 | 16 | 85895099 | upstream gene variant | C/G | snv | 7.9E-02 | 2 | ||||
rs12232384 | 16 | 85976154 | intron variant | C/A;T | snv | 2 | |||||
rs12898000 | 14 | 103368791 | upstream gene variant | G/C;T | snv | 2 | |||||
rs12916091 | 15 | 79930230 | downstream gene variant | T/G | snv | 0.53 | 2 | ||||
rs12973608 | 19 | 18287220 | upstream gene variant | A/C;G | snv | 2 | |||||
rs13022141 | 2 | 136131638 | intergenic variant | A/G | snv | 0.69 | 2 | ||||
rs140058837 | 3 | 46313128 | upstream gene variant | A/G | snv | 2.2E-02 | 2 | ||||
rs1400745 | 14 | 34886094 | intergenic variant | A/G | snv | 0.41 | 2 | ||||
rs142105922 | 16 | 85968988 | intron variant | TAATAA/-;TAA;TAATAATAA;TAATAATAATAA;TAATAATAATAATAA | delins | 2 | |||||
rs144110170 | 11 | 122649353 | regulatory region variant | C/- | delins | 0.13 | 2 | ||||
rs146723115 | 8 | 67901594 | intergenic variant | AT/-;ATAT;ATATAT;ATATTTATATATAATATATATAATTTATATATATATATATAT | delins | 2 | |||||
rs150861794 | 13 | 108351457 | intron variant | C/T | snv | 1.7E-02 | 2 | ||||
rs199741557 | 4 | 104943373 | intron variant | TC/- | delins | 2.6E-02 | 2 | ||||
rs200516372 | 3 | 141484141 | upstream gene variant | A/G | snv | 2.4E-02 | 2 |