Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
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 | ||
rs1256580 | 1.000 | 0.040 | 1 | 219026038 | intron variant | G/C | snv | 0.29 | 1 | ||
rs1533326 | 1.000 | 0.040 | 15 | 90211722 | intron variant | A/G | snv | 0.39 | 1 | ||
rs158639 | 1.000 | 0.040 | 5 | 56315883 | intron variant | G/A | snv | 0.33 | 1 | ||
rs17651189 | 1.000 | 0.040 | 22 | 24448915 | intron variant | T/C | snv | 2.9E-02 | 1 | ||
rs2727365 | 1.000 | 0.040 | 11 | 13089937 | intron variant | G/A;T | snv | 1 | |||
rs28360612 | 1.000 | 0.040 | 22 | 24487250 | intron variant | T/A | snv | 0.20 | 1 | ||
rs28405582 | 1.000 | 0.040 | 3 | 23863271 | intron variant | T/C | snv | 4.6E-02 | 1 | ||
rs28570522 | 1.000 | 0.040 | 8 | 10773058 | intron variant | A/G | snv | 0.66 | 1 | ||
rs330071 | 1.000 | 0.040 | 8 | 9302385 | intron variant | G/A | snv | 0.25 | 1 | ||
rs72966077 | 1.000 | 0.040 | 2 | 218894507 | intron variant | C/T | snv | 3.3E-02 | 1 | ||
rs7531806 | 1.000 | 0.040 | 1 | 169681903 | intron variant | G/A | snv | 0.61 | 1 | ||
rs75430906 | 1.000 | 0.040 | 3 | 20676437 | intron variant | G/A | snv | 1.9E-02 | 1 | ||
rs7809981 | 1.000 | 0.040 | 7 | 40834777 | intron variant | G/T | snv | 0.24 | 1 | ||
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 | ||
rs11118336 | 1.000 | 0.040 | 1 | 219547941 | intergenic variant | C/T | snv | 0.51 | 1 | ||
rs2901000 | 1.000 | 0.040 | 2 | 60274081 | intergenic variant | A/G | snv | 0.62 | 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 | ||
rs1159268 | 1.000 | 0.040 | 1 | 218671564 | regulatory region variant | G/A | snv | 0.32 | 1 | ||
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 |