Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4420638 | 0.708 | 0.520 | 19 | 44919689 | downstream gene variant | A/G | snv | 0.18 | 30 | ||
rs1800437 | 0.827 | 0.160 | 19 | 45678134 | missense variant | G/C | snv | 0.18 | 0.17 | 9 | |
rs2074356 | 0.763 | 0.280 | 12 | 112207597 | intron variant | G/A | snv | 3.8E-03 | 9 | ||
rs2925979 | 1.000 | 0.080 | 16 | 81501185 | intron variant | T/A;C | snv | 9 | |||
rs459193 | 0.925 | 0.120 | 5 | 56510924 | downstream gene variant | A/G | snv | 0.69 | 9 | ||
rs2820443 | 0.882 | 0.120 | 1 | 219580167 | regulatory region variant | T/C | snv | 0.23 | 8 | ||
rs12454712 | 0.925 | 0.120 | 18 | 63178651 | intron variant | T/A;C | snv | 7 | |||
rs7607980 | 1.000 | 0.080 | 2 | 164694691 | missense variant | T/C | snv | 0.11 | 0.13 | 7 | |
rs10195252 | 0.925 | 0.080 | 2 | 164656581 | intron variant | T/C | snv | 0.48 | 6 | ||
rs6795735 | 0.882 | 0.120 | 3 | 64719689 | intron variant | C/A;G;T | snv | 6 | |||
rs13389219 | 1.000 | 0.080 | 2 | 164672366 | intron variant | C/T | snv | 0.47 | 5 | ||
rs3786897 | 1.000 | 0.080 | 19 | 33402102 | intron variant | A/G | snv | 0.45 | 5 | ||
rs9844972 | 1.000 | 0.080 | 3 | 150379848 | regulatory region variant | G/A;C | snv | 4 | |||
rs35169799 | 0.925 | 0.200 | 11 | 64263769 | missense variant | C/T | snv | 4.9E-02 | 4.5E-02 | 3 | |
rs3764002 | 1.000 | 0.080 | 12 | 108224853 | missense variant | C/T | snv | 0.27 | 0.20 | 3 | |
rs10260148 | 1.000 | 0.080 | 7 | 130746210 | intergenic variant | C/T | snv | 0.27 | 2 | ||
rs622217 | 1.000 | 0.080 | 6 | 160345738 | upstream gene variant | T/A;C | snv | 2 | |||
rs757110 | 0.851 | 0.080 | 11 | 17396930 | missense variant | C/A;T | snv | 0.64; 8.0E-06 | 2 | ||
rs9369425 | 0.882 | 0.160 | 6 | 43843237 | downstream gene variant | G/A | snv | 0.66 | 2 |