Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 24 | ||
rs653178 | 0.672 | 0.600 | 12 | 111569952 | intron variant | C/T | snv | 0.67 | 17 | ||
rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 14 | |
rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 13 | |
rs11065987 | 0.807 | 0.280 | 12 | 111634620 | intergenic variant | A/G | snv | 0.29 | 12 | ||
rs17696736 | 0.827 | 0.240 | 12 | 112049014 | intron variant | A/G | snv | 0.30 | 11 | ||
rs2516049 | 0.742 | 0.400 | 6 | 32602623 | intergenic variant | T/C | snv | 0.27 | 9 | ||
rs477515 | 0.790 | 0.400 | 6 | 32601914 | intergenic variant | G/A | snv | 0.27 | 7 | ||
rs3087243 | 0.623 | 0.720 | 2 | 203874196 | downstream gene variant | G/A | snv | 0.37 | 6 | ||
rs6679677 | 0.653 | 0.320 | 1 | 113761186 | upstream gene variant | C/A | snv | 6.7E-02 | 6 | ||
rs925489 | 0.882 | 0.080 | 9 | 97784318 | intron variant | C/T | snv | 0.71 | 5 | ||
rs3129720 | 0.851 | 0.280 | 6 | 32695854 | intergenic variant | T/C | snv | 0.76 | 4 | ||
rs10774625 | 0.763 | 0.320 | 12 | 111472415 | intron variant | A/G | snv | 0.66 | 4 | ||
rs11066188 | 0.851 | 0.320 | 12 | 112172910 | intron variant | G/A;C | snv | 0.30; 4.1E-06 | 4 | ||
rs965513 | 0.742 | 0.200 | 9 | 97793827 | intron variant | A/G;T | snv | 4 | |||
rs11066320 | 0.925 | 0.120 | 12 | 112468611 | intron variant | A/G | snv | 0.70 | 4 | ||
rs34536443 | 0.667 | 0.400 | 19 | 10352442 | missense variant | G/C | snv | 2.7E-02 | 2.8E-02 | 4 | |
rs4409785 | 0.752 | 0.240 | 11 | 95578258 | intron variant | T/C | snv | 0.13 | 3 | ||
rs6906021 | 0.827 | 0.320 | 6 | 32658534 | upstream gene variant | T/C | snv | 0.47 | 3 | ||
rs10759944 | 0.925 | 0.080 | 9 | 97794690 | intron variant | A/G | snv | 0.72 | 3 | ||
rs1443438 | 0.827 | 0.080 | 9 | 97787746 | intron variant | T/A;C | snv | 3 | |||
rs7850258 | 0.827 | 0.200 | 9 | 97786731 | intron variant | A/G | snv | 0.72 | 3 | ||
rs6910071 | 0.790 | 0.320 | 6 | 32315077 | intron variant | A/G | snv | 0.14 | 3 | ||
rs10984103 | 0.925 | 0.080 | 9 | 97876993 | TF binding site variant | A/C | snv | 0.68 | 2 | ||
rs12191243 | 1.000 | 0.040 | 6 | 135125688 | intergenic variant | C/G | snv | 0.20 | 2 |