Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs543874 | 1.000 | 0.080 | 1 | 177920345 | upstream gene variant | A/G | snv | 0.21 | 11 | ||
rs2568958 | 0.882 | 0.160 | 1 | 72299433 | intron variant | G/A;C | snv | 8 | |||
rs10913469 | 1.000 | 0.080 | 1 | 177944384 | intron variant | T/C | snv | 0.22 | 7 | ||
rs2815752 | 0.925 | 0.200 | 1 | 72346757 | intron variant | G/A | snv | 0.62 | 7 | ||
rs633715 | 1.000 | 0.080 | 1 | 177883445 | intron variant | T/C | snv | 0.17 | 7 | ||
rs11161721 | 1 | 86022231 | intron variant | C/A | snv | 0.27 | 0.27 | 4 | |||
rs1514175 | 1.000 | 0.080 | 1 | 74525960 | intron variant | A/G | snv | 0.48 | 4 | ||
rs10789336 | 1 | 72372723 | intron variant | G/A;C | snv | 3 | |||||
rs113722913 | 1 | 199950846 | intergenic variant | T/C | snv | 2.6E-02 | 3 | ||||
rs1555543 | 1 | 96479241 | intergenic variant | A/C | snv | 0.55 | 3 | ||||
rs17124318 | 1 | 63015059 | intron variant | C/A;G;T | snv | 3 | |||||
rs2785980 | 1 | 219527177 | intergenic variant | T/C | snv | 0.28 | 3 | ||||
rs3934834 | 1 | 1070426 | downstream gene variant | C/T | snv | 0.21 | 3 | ||||
rs516636 | 1 | 177886382 | intron variant | C/A | snv | 0.17 | 3 | ||||
rs574367 | 1 | 177904075 | intron variant | G/T | snv | 0.16 | 3 | ||||
rs591120 | 1 | 177933618 | missense variant | G/A;C | snv | 4.0E-06; 0.42 | 3 | ||||
rs6689335 | 1 | 219455340 | intron variant | T/C | snv | 0.31 | 3 | ||||
rs113313252 | 1 | 74534327 | intron variant | -/T | delins | 2 | |||||
rs12142020 | 1 | 74534327 | intron variant | A/T | snv | 0.50 | 2 | ||||
rs201167096 | 1 | 74534327 | intron variant | -/T | delins | 2 | |||||
rs780094 | 0.658 | 0.400 | 2 | 27518370 | intron variant | T/C | snv | 0.67 | 62 | ||
rs2943634 | 0.763 | 0.200 | 2 | 226203364 | intergenic variant | A/C;G | snv | 15 | |||
rs2068834 | 0.925 | 0.120 | 2 | 27616672 | intron variant | T/C | snv | 0.28 | 10 | ||
rs6548238 | 0.882 | 0.200 | 2 | 634905 | TF binding site variant | T/C | snv | 0.85 | 10 | ||
rs2867125 | 0.925 | 0.120 | 2 | 622827 | intergenic variant | T/A;C | snv | 0.85 | 8 |