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 | ||
rs1047891 | 0.827 | 0.200 | 2 | 210675783 | missense variant | C/A | snv | 0.30 | 0.33 | 8 | |
rs7681423 | 4 | 154621096 | intergenic variant | C/T | snv | 0.26 | 5 | ||||
rs6050 | 0.827 | 0.120 | 4 | 154586438 | missense variant | T/A;C | snv | 0.29 | 5 | ||
rs2066861 | 4 | 154606284 | intron variant | C/T | snv | 0.26 | 5 | ||||
rs1800961 | 0.851 | 0.160 | 20 | 44413724 | missense variant | C/T | snv | 3.1E-02 | 2.5E-02 | 5 | |
rs2228145 | 0.602 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 0.38; 1.2E-05 | 5 | ||
rs4129267 | 0.807 | 0.200 | 1 | 154453788 | intron variant | C/G;T | snv | 5 | |||
rs6734238 | 1.000 | 0.080 | 2 | 113083453 | upstream gene variant | A/G | snv | 0.39 | 4 | ||
rs4537545 | 0.790 | 0.160 | 1 | 154446403 | intron variant | C/T | snv | 0.48 | 4 | ||
rs7518199 | 1 | 154434943 | intron variant | A/C;T | snv | 0.39; 4.2E-06 | 4 | ||||
rs7529229 | 0.851 | 0.120 | 1 | 154448302 | intron variant | T/C | snv | 0.48 | 4 | ||
rs7232 | 1.000 | 0.080 | 11 | 60173126 | missense variant | T/A | snv | 0.31 | 0.27 | 4 | |
rs12239046 | 1 | 247438293 | intron variant | T/C | snv | 0.58 | 4 | ||||
rs2073643 | 1.000 | 0.080 | 5 | 132387596 | intron variant | T/C | snv | 0.46 | 4 | ||
rs2158177 | 0.925 | 0.120 | 5 | 132648366 | intron variant | A/G | snv | 0.18 | 4 | ||
rs10034922 | 4 | 154599476 | downstream gene variant | G/A | snv | 5.2E-02 | 3 | ||||
rs1016988 | 5 | 132408882 | upstream gene variant | T/C | snv | 0.20 | 3 | ||||
rs10226084 | 7 | 17957989 | upstream gene variant | T/C | snv | 0.46 | 3 | ||||
rs1154988 | 3 | 136206349 | upstream gene variant | T/A | snv | 0.76 | 3 | ||||
rs12511469 | 4 | 154530607 | downstream gene variant | T/A | snv | 0.18 | 3 | ||||
rs17690122 | 5 | 132532143 | intron variant | A/G;T | snv | 3 | |||||
rs1938492 | 1 | 65652146 | intergenic variant | A/C | snv | 0.43 | 3 | ||||
rs434943 | 14 | 68847342 | intergenic variant | G/A | snv | 0.27 | 3 | ||||
rs4463047 | 4 | 154574381 | downstream gene variant | T/C | snv | 0.15 | 3 |