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 | ||
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 | ||
rs11066188 | 0.851 | 0.320 | 12 | 112172910 | intron variant | G/A;C | snv | 0.30; 4.1E-06 | 4 | ||
rs11066320 | 0.925 | 0.120 | 12 | 112468611 | intron variant | A/G | snv | 0.70 | 4 | ||
rs1801133 | 0.472 | 0.880 | 1 | 11796321 | missense variant | G/A | snv | 0.31 | 0.27 | 3 | |
rs1857231 | 1.000 | 0.080 | 10 | 8919651 | intergenic variant | G/A | snv | 0.64 | 1 | ||
rs6499100 | 1.000 | 0.080 | 16 | 52797550 | intergenic variant | T/C | snv | 0.42 | 1 | ||
rs1800469 | 0.547 | 0.760 | 19 | 41354391 | intron variant | A/G | snv | 0.69 | 1 | ||
rs7982677 | 1.000 | 0.080 | 13 | 92336070 | intron variant | C/A | snv | 0.29 | 1 | ||
rs4771856 | 1.000 | 0.080 | 13 | 92342256 | intron variant | C/A | snv | 0.29 | 1 | ||
rs2388896 | 1.000 | 0.080 | 10 | 8912261 | intron variant | A/G | snv | 0.64 | 1 | ||
rs2228638 | 1.000 | 0.080 | 10 | 33186354 | missense variant | C/T | snv | 0.12 | 9.4E-02 | 1 | |
rs233716 | 1.000 | 0.080 | 12 | 112602139 | intron variant | C/T | snv | 0.58 | 1 | ||
rs233722 | 1.000 | 0.080 | 12 | 112593670 | intron variant | G/A | snv | 0.53 | 1 |