Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1801282 | 0.500 | 0.840 | 3 | 12351626 | missense variant | C/G | snv | 0.11 | 8.9E-02 | 131 | |
rs1805192 | 0.510 | 0.840 | 3 | 12379739 | missense variant | C/G | snv | 121 | |||
rs5743708 | 0.525 | 0.800 | 4 | 153705165 | missense variant | G/A | snv | 1.7E-02 | 1.8E-02 | 98 | |
rs7799039 | 0.649 | 0.560 | 7 | 128238730 | upstream gene variant | G/A;C | snv | 33 | |||
rs1061622 | 0.633 | 0.760 | 1 | 12192898 | missense variant | T/G | snv | 0.22 | 0.22 | 33 | |
rs10754558 | 0.695 | 0.480 | 1 | 247448734 | 3 prime UTR variant | G/C;T | snv | 20 | |||
rs121908120 | 0.701 | 0.280 | 2 | 218890289 | missense variant | T/A | snv | 1.4E-02 | 1.4E-02 | 19 | |
rs34560261 | 0.882 | 0.040 | 15 | 90191194 | intron variant | C/T | snv | 0.12 | 3 | ||
rs6428829 | 0.925 | 0.040 | 1 | 119512118 | intron variant | A/G | snv | 0.78 | 2 | ||
rs10911268 | 1.000 | 0.040 | 1 | 183153583 | intergenic variant | C/A | snv | 0.39 | 1 | ||
rs1092479 | 1.000 | 0.040 | 2 | 121011861 | intergenic variant | G/C | snv | 0.39 | 1 | ||
rs1159268 | 1.000 | 0.040 | 1 | 218671564 | regulatory region variant | G/A | snv | 0.32 | 1 | ||
rs2727365 | 1.000 | 0.040 | 11 | 13089937 | intron variant | G/A;T | snv | 1 | |||
rs2901000 | 1.000 | 0.040 | 2 | 60274081 | intergenic variant | A/G | snv | 0.62 | 1 | ||
rs330071 | 1.000 | 0.040 | 8 | 9302385 | intron variant | G/A | snv | 0.25 | 1 | ||
rs38055 | 1.000 | 0.040 | 5 | 53264814 | intergenic variant | A/G | snv | 0.75 | 1 | ||
rs4487353 | 1.000 | 0.040 | 4 | 123332634 | intergenic variant | G/A | snv | 0.53 | 1 | ||
rs478304 | 1.000 | 0.040 | 11 | 65726789 | upstream gene variant | G/T | snv | 0.54 | 1 | ||
rs629725 | 1.000 | 0.040 | 5 | 53335237 | TF binding site variant | T/C | snv | 0.74 | 1 | ||
rs6684868 | 1.000 | 0.040 | 1 | 218674648 | TF binding site variant | G/A | snv | 0.41 | 1 | ||
rs75430906 | 1.000 | 0.040 | 3 | 20676437 | intron variant | G/A | snv | 1.9E-02 | 1 | ||
rs788790 | 1.000 | 0.040 | 1 | 202320478 | downstream gene variant | C/A | snv | 0.44 | 1 | ||
rs17651189 | 1.000 | 0.040 | 22 | 24448915 | intron variant | T/C | snv | 2.9E-02 | 1 | ||
rs28360612 | 1.000 | 0.040 | 22 | 24487250 | intron variant | T/A | snv | 0.20 | 1 | ||
rs747650 | 1.000 | 0.040 | 11 | 47154454 | non coding transcript exon variant | C/T | snv | 0.34 | 1 |