Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10078021 | 5 | 75742606 | intergenic variant | T/G | snv | 0.51 | 1 | ||||
rs10103353 | 8 | 81937217 | intergenic variant | C/T | snv | 0.35 | 1 | ||||
rs1015291 | 12 | 19831845 | intron variant | A/G | snv | 0.55 | 1 | ||||
rs10184839 | 2 | 181081388 | intron variant | A/T | snv | 0.77 | 1 | ||||
rs1040922 | 20 | 10787163 | intron variant | G/T | snv | 0.27 | 1 | ||||
rs10751962 | 10 | 4130519 | intergenic variant | C/G;T | snv | 1 | |||||
rs1081707 | 2 | 96381261 | downstream gene variant | G/A | snv | 0.24 | 1 | ||||
rs10822407 | 10 | 65024342 | intergenic variant | T/C | snv | 0.30 | 1 | ||||
rs10864859 | 2 | 120682642 | downstream gene variant | G/C;T | snv | 1 | |||||
rs1098708 | 12 | 27168179 | intergenic variant | A/G | snv | 0.35 | 1 | ||||
rs11022734 | 11 | 13260033 | intergenic variant | A/G | snv | 0.64 | 1 | ||||
rs111304266 | 5 | 57293715 | intergenic variant | C/G | snv | 2.7E-02 | 1 | ||||
rs113134141 | 3 | 46820449 | intergenic variant | A/G | snv | 0.17 | 1 | ||||
rs114503346 | 5 | 172765347 | intron variant | C/T | snv | 2.7E-02 | 1 | ||||
rs115234772 | 2 | 53423157 | TF binding site variant | A/G | snv | 3.7E-03 | 1 | ||||
rs115726563 | 6 | 31098642 | intergenic variant | C/T | snv | 1 | |||||
rs11628933 | 14 | 60234185 | intergenic variant | G/C;T | snv | 1 | |||||
rs11671323 | 19 | 21696775 | intergenic variant | A/G | snv | 0.41 | 1 | ||||
rs11681462 | 2 | 42125427 | intergenic variant | A/C | snv | 0.15 | 1 | ||||
rs117059939 | 14 | 36401137 | intron variant | G/T | snv | 9.5E-03 | 1 | ||||
rs11780200 | 8 | 119446281 | intron variant | G/A | snv | 0.19 | 1 | ||||
rs11923667 | 3 | 101549236 | regulatory region variant | T/A | snv | 0.40 | 1 | ||||
rs11931572 | 4 | 30084482 | intergenic variant | A/C | snv | 1.6E-02 | 1 | ||||
rs1220128 | 2 | 157643390 | intergenic variant | G/A;C | snv | 1 | |||||
rs1240716 | 1 | 1410616 | non coding transcript exon variant | G/A;T | snv | 1 |