Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs9557321 | 1.000 | 0.120 | 13 | 99868847 | intron variant | T/C | snv | 3.8E-02 | 1 | ||
rs11761528 | 1.000 | 0.120 | 7 | 99521178 | intron variant | C/T | snv | 0.12 | 4 | ||
rs372329931 | 1.000 | 0.120 | 4 | 99435310 | 5 prime UTR variant | T/C | snv | 4.3E-04 | 3.6E-04 | 2 | |
rs740160 | 1.000 | 0.120 | 7 | 99360257 | intron variant | C/T | snv | 8.6E-02 | 2 | ||
rs337527 | 1.000 | 0.120 | 9 | 98685681 | intron variant | T/C | snv | 3.9E-02 | 1 | ||
rs111988552 | 1.000 | 0.120 | 4 | 98557163 | intron variant | A/T | snv | 1 | |||
rs1052133 | 0.476 | 0.800 | 3 | 9757089 | missense variant | C/G | snv | 0.27 | 0.22 | 147 | |
rs746702110 | 0.627 | 0.480 | 3 | 9756778 | missense variant | C/T | snv | 1.2E-05 | 2.8E-05 | 38 | |
rs3219008 | 1.000 | 0.120 | 3 | 9753859 | intron variant | A/G | snv | 0.28 | 1 | ||
rs159153 | 1.000 | 0.120 | 3 | 9748191 | upstream gene variant | T/C | snv | 0.32 | 1 | ||
rs13101828 | 0.851 | 0.160 | 4 | 971932 | intron variant | A/G | snv | 0.43 | 6 | ||
rs2274795 | 1.000 | 0.120 | 14 | 96528345 | intron variant | T/C | snv | 0.26 | 1 | ||
rs10520789 | 1.000 | 0.120 | 15 | 95598638 | regulatory region variant | G/A | snv | 0.12 | 1 | ||
rs4409785 | 0.752 | 0.240 | 11 | 95578258 | intron variant | T/C | snv | 0.13 | 12 | ||
rs854560 | 0.513 | 0.800 | 7 | 95316772 | missense variant | A/C;G;N;T | snv | 0.29 | 113 | ||
rs662 | 0.485 | 0.840 | 7 | 95308134 | missense variant | T/C | snv | 0.38 | 0.42 | 157 | |
rs3765534 | 0.882 | 0.200 | 13 | 95163161 | missense variant | C/T | snv | 2.3E-02 | 1.2E-02 | 4 | |
rs11121380 | 1.000 | 0.120 | 1 | 9348900 | intron variant | A/C | snv | 0.11 | 1 | ||
rs42041 | 0.882 | 0.280 | 7 | 92617430 | intron variant | C/G | snv | 0.21 | 3 | ||
rs4272 | 1.000 | 0.120 | 7 | 92607515 | 3 prime UTR variant | A/G;T | snv | 3 | |||
rs9909240 | 1.000 | 0.120 | 17 | 9236774 | intron variant | G/A | snv | 0.50 | 1 | ||
rs9516053 | 1.000 | 0.120 | 13 | 92293631 | intron variant | T/A;C | snv | 1 | |||
rs7164176 | 1.000 | 0.120 | 15 | 91668544 | intergenic variant | G/A | snv | 0.65 | 1 | ||
rs284515 | 1.000 | 0.120 | 6 | 90499109 | intergenic variant | A/G | snv | 0.12 | 1 | ||
rs284511 | 1.000 | 0.120 | 6 | 90498823 | intergenic variant | T/A;C | snv | 1 |