Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11206510 | 0.763 | 0.240 | 1 | 55030366 | intergenic variant | T/A;C;G | snv | 4 | |||
rs11556924 | 0.752 | 0.240 | 7 | 130023656 | missense variant | C/A;T | snv | 4.0E-06; 0.28 | 13 | ||
rs17465637 | 0.790 | 0.200 | 1 | 222650187 | intron variant | A/C;G;T | snv | 0.64; 6.4E-06 | 3 | ||
rs2895811 | 0.851 | 0.080 | 14 | 99667605 | intron variant | T/A;C | snv | 2 | |||
rs2943634 | 0.763 | 0.200 | 2 | 226203364 | intergenic variant | A/C;G | snv | 5 | |||
rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 61 | ||
rs4977574 | 0.695 | 0.520 | 9 | 22098575 | intron variant | A/G;T | snv | 3 | |||
rs6841581 | 0.882 | 0.080 | 4 | 147480038 | upstream gene variant | G/A;T | snv | 3 | |||
rs974819 | 0.807 | 0.080 | 11 | 103789839 | intron variant | T/A;C | snv | 2 | |||
rs186696265 | 0.882 | 0.040 | 6 | 160690668 | intergenic variant | C/T | snv | 1.0E-02 | 6 | ||
rs10455872 | 0.662 | 0.320 | 6 | 160589086 | intron variant | A/G | snv | 4.3E-02 | 10 | ||
rs7412 | 0.641 | 0.640 | 19 | 44908822 | missense variant | C/T | snv | 6.2E-02 | 7.9E-02 | 20 | |
rs17114046 | 0.925 | 0.040 | 1 | 56500678 | intron variant | A/G | snv | 0.12 | 2 | ||
rs264 | 0.882 | 0.080 | 8 | 19955669 | intron variant | G/A | snv | 0.14 | 2 | ||
rs11057830 | 0.851 | 0.040 | 12 | 124822507 | intron variant | G/A | snv | 0.15 | 4 | ||
rs4420638 | 0.708 | 0.520 | 19 | 44919689 | downstream gene variant | A/G | snv | 0.18 | 30 | ||
rs2107595 | 0.732 | 0.280 | 7 | 19009765 | regulatory region variant | G/A | snv | 0.19 | 8 | ||
rs12740374 | 0.851 | 0.040 | 1 | 109274968 | 3 prime UTR variant | G/T | snv | 0.22 | 9 | ||
rs7528419 | 0.851 | 0.080 | 1 | 109274570 | 3 prime UTR variant | A/G | snv | 0.23 | 9 | ||
rs9349379 | 0.732 | 0.200 | 6 | 12903725 | intron variant | A/G | snv | 0.32 | 8 | ||
rs216172 | 0.925 | 0.040 | 17 | 2223210 | intron variant | G/C | snv | 0.35 | 2 | ||
rs1412444 | 0.851 | 0.120 | 10 | 89243170 | intron variant | C/T | snv | 0.37 | 2 | ||
rs12936587 | 0.882 | 0.080 | 17 | 17640408 | regulatory region variant | G/A | snv | 0.38 | 4 | ||
rs1333049 | 0.614 | 0.520 | 9 | 22125504 | intron variant | G/C | snv | 0.41 | 18 | ||
rs7173743 | 0.851 | 0.120 | 15 | 78849442 | intron variant | T/C | snv | 0.45 | 2 |