Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10019658 | 1.000 | 0.040 | 4 | 34423326 | intergenic variant | A/G | snv | 0.22 | 1 | ||
rs12309467 | 1.000 | 0.040 | 12 | 83644699 | intergenic variant | C/A;G | snv | 1 | |||
rs148639588 | 1.000 | 0.040 | 1 | 102806868 | intron variant | T/C | snv | 1 | |||
rs16886018 | 1.000 | 0.040 | 5 | 56682224 | intergenic variant | C/A | snv | 6.3E-02 | 1 | ||
rs2487032 | 1.000 | 0.040 | 9 | 104941653 | regulatory region variant | G/A | snv | 0.58 | 1 | ||
rs2627761 | 1.000 | 0.040 | 2 | 55705879 | intergenic variant | C/T | snv | 0.84 | 1 | ||
rs3012455 | 1.000 | 0.040 | 6 | 170132792 | upstream gene variant | A/G | snv | 0.94 | 1 | ||
rs327636 | 1.000 | 0.040 | 7 | 81219506 | intergenic variant | A/G | snv | 0.56 | 1 | ||
rs34935520 | 1.000 | 0.040 | 14 | 60624683 | intergenic variant | G/A | snv | 0.45 | 1 | ||
rs35155027 | 1.000 | 0.040 | 14 | 60628456 | intergenic variant | G/C;T | snv | 0.45 | 1 | ||
rs4492904 | 1.000 | 0.040 | 12 | 70987768 | intergenic variant | C/A | snv | 9.9E-02 | 1 | ||
rs56335522 | 1.000 | 0.040 | 2 | 212893510 | intron variant | G/A;C;T | snv | 1 | |||
rs58714937 | 1.000 | 0.040 | 22 | 19869187 | regulatory region variant | C/T | snv | 0.26 | 1 | ||
rs6573307 | 1.000 | 0.040 | 14 | 60331291 | TF binding site variant | T/A;G | snv | 1 | |||
rs67530707 | 1.000 | 0.040 | 6 | 36625210 | upstream gene variant | AC/- | delins | 1 | |||
rs6947612 | 1.000 | 0.040 | 7 | 117992921 | intergenic variant | A/G;T | snv | 1 | |||
rs6969706 | 1.000 | 0.040 | 7 | 116514777 | intergenic variant | G/C;T | snv | 1 | |||
rs72815193 | 1.000 | 0.040 | 10 | 93203634 | downstream gene variant | A/G | snv | 0.37 | 1 | ||
rs7389781 | 1.000 | 0.040 | 9 | 35573945 | intergenic variant | T/A | snv | 0.67 | 1 | ||
rs3789134 | 1.000 | 0.040 | 2 | 110922578 | intron variant | T/C | snv | 0.31 | 1 | ||
rs59521811 | 1.000 | 0.040 | 4 | 7908045 | intron variant | T/C | snv | 0.38 | 1 | ||
rs6857814 | 1.000 | 0.040 | 4 | 7914813 | intron variant | A/G | snv | 0.57 | 1 | ||
rs9330348 | 1.000 | 0.040 | 4 | 7882160 | intron variant | C/G | snv | 0.43 | 1 | ||
rs2514882 | 1.000 | 0.040 | 8 | 107263553 | intron variant | C/T | snv | 0.85 | 1 | ||
rs76325372 | 1.000 | 0.040 | 5 | 14837223 | intron variant | A/C;T | snv | 1 |