Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10811661 | 0.724 | 0.400 | 9 | 22134095 | intergenic variant | T/C | snv | 0.14 | 22 | ||
rs1800764 | 0.790 | 0.320 | 17 | 63473168 | upstream gene variant | C/G;T | snv | 10 | |||
rs3865188 | 0.790 | 0.320 | 16 | 82617112 | intergenic variant | A/G;T | snv | 10 | |||
rs11646213 | 0.827 | 0.320 | 16 | 82609046 | intergenic variant | A/T | snv | 0.47 | 6 | ||
rs12449782 | 0.925 | 0.200 | 17 | 63498888 | intron variant | G/A | snv | 0.41 | 3 | ||
rs16835198 | 0.882 | 0.200 | 1 | 32861080 | downstream gene variant | G/T | snv | 0.29 | 3 | ||
rs955333 | 0.882 | 0.240 | 6 | 154626274 | intergenic variant | A/G | snv | 0.13 | 3 | ||
rs10255208 | 0.925 | 0.160 | 7 | 36819038 | non coding transcript exon variant | A/G | snv | 0.46 | 2 | ||
rs17300593 | 0.925 | 0.160 | 1 | 58637536 | intergenic variant | C/G | snv | 2 | |||
rs1942872 | 0.925 | 0.160 | 18 | 60201132 | downstream gene variant | C/T | snv | 0.21 | 2 | ||
rs2874116 | 0.925 | 0.160 | 18 | 58792367 | regulatory region variant | G/A | snv | 0.36 | 2 | ||
rs488846 | 0.925 | 0.160 | 18 | 54261400 | intergenic variant | T/C | snv | 0.26 | 2 | ||
rs499765 | 0.925 | 0.160 | 19 | 48763133 | downstream gene variant | C/G | snv | 0.45 | 2 | ||
rs6704078 | 0.925 | 0.200 | 1 | 216437370 | intergenic variant | C/T | snv | 0.94 | 2 | ||
rs9942471 | 0.925 | 0.160 | 6 | 89238513 | intergenic variant | A/C | snv | 0.37 | 2 | ||
rs10952362 | 1.000 | 0.120 | 7 | 152565713 | regulatory region variant | T/C | snv | 0.25 | 1 | ||
rs11886047 | 1.000 | 0.120 | 2 | 43623451 | upstream gene variant | T/A;C | snv | 0.20 | 1 | ||
rs1249910 | 1.000 | 0.120 | 3 | 112672327 | intergenic variant | A/G | snv | 0.58 | 1 | ||
rs12523822 | 1.000 | 0.120 | 6 | 154633286 | intergenic variant | C/G;T | snv | 1 | |||
rs1253192 | 1.000 | 0.120 | 14 | 59376688 | intergenic variant | A/G | snv | 0.92 | 1 | ||
rs16996381 | 1.000 | 0.120 | 22 | 36115231 | intergenic variant | G/A | snv | 0.31 | 1 | ||
rs1866813 | 1.000 | 0.120 | 3 | 137083096 | intergenic variant | A/C | snv | 0.14 | 1 | ||
rs334543 | 1.000 | 0.120 | 3 | 120113774 | intron variant | C/A | snv | 0.74 | 1 | ||
rs11887534 | 0.653 | 0.440 | 2 | 43839108 | missense variant | G/A;C | snv | 6.4E-06; 6.7E-02 | 29 | ||
rs2268388 | 0.851 | 0.200 | 12 | 109205840 | intron variant | G/A | snv | 0.14 | 6 |