Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2954021 | 1.000 | 0.040 | 8 | 125469835 | intron variant | A/G | snv | 0.54 | 13 | ||
rs495828 | 0.827 | 0.200 | 9 | 133279294 | upstream gene variant | T/G | snv | 0.81 | 11 | ||
rs651007 | 0.851 | 0.160 | 9 | 133278431 | upstream gene variant | T/A;C | snv | 11 | |||
rs579459 | 0.752 | 0.320 | 9 | 133278724 | upstream gene variant | C/T | snv | 0.81 | 10 | ||
rs10819937 | 9 | 101460951 | intergenic variant | C/G;T | snv | 1 | |||||
rs1780324 | 1 | 21495264 | intergenic variant | A/G | snv | 0.48 | 1 | ||||
rs36053309 | 1 | 21579111 | downstream gene variant | C/G;T | snv | 0.21 | 1 | ||||
rs6984305 | 8 | 9320758 | intron variant | A/T | snv | 0.85 | 1 | ||||
rs7025162 | 1.000 | 0.080 | 9 | 133290774 | regulatory region variant | T/C | snv | 0.82 | 1 | ||
rs7173947 | 15 | 94727238 | upstream gene variant | C/T | snv | 0.61 | 1 | ||||
rs7186908 | 16 | 72186474 | regulatory region variant | G/C | snv | 0.26 | 1 | ||||
rs72837690 | 17 | 7185104 | downstream gene variant | T/C | snv | 0.31 | 1 | ||||
rs73766540 | 5 | 82427213 | intergenic variant | T/A;C | snv | 1 | |||||
rs75432325 | 17 | 49872966 | regulatory region variant | T/A;C | snv | 1 | |||||
rs9533177 | 13 | 42615089 | intergenic variant | G/T | snv | 0.40 | 1 | ||||
rs16856332 | 2 | 168984064 | intron variant | T/A;G | snv | 1 | |||||
rs7267979 | 20 | 25317451 | intron variant | A/G | snv | 0.58 | 1 | ||||
rs2519093 | 0.882 | 0.200 | 9 | 133266456 | intron variant | T/C | snv | 14 | |||
rs505922 | 0.689 | 0.520 | 9 | 133273813 | intron variant | C/T | snv | 11 | |||
rs657152 | 0.882 | 0.200 | 9 | 133263862 | intron variant | A/C;T | snv | 6 | |||
rs8176720 | 9 | 133257486 | synonymous variant | T/A;C;G | snv | 0.40 | 0.40 | 2 | |||
rs79343853 | 9 | 133270880 | intron variant | T/C | snv | 1 | |||||
rs4962153 | 0.925 | 0.120 | 9 | 133458632 | intron variant | A/G | snv | 0.79 | 4 | ||
rs150674717 | 6 | 24512970 | intron variant | G/A | snv | 2.0E-04 | 1 | ||||
rs2242420 | 1 | 21578036 | 3 prime UTR variant | C/T | snv | 0.11 | 1 |