Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12232497 | 0.701 | 0.360 | 17 | 39883866 | intergenic variant | T/C | snv | 0.35 | 3 | ||
rs7216389 | 0.732 | 0.440 | 17 | 39913696 | intron variant | C/T | snv | 0.60 | 3 | ||
rs7927894 | 0.742 | 0.320 | 11 | 76590272 | upstream gene variant | C/T | snv | 0.35 | 5 | ||
rs2872507 | 0.752 | 0.360 | 17 | 39884510 | intergenic variant | G/A;T | snv | 7 | |||
rs8067378 | 0.752 | 0.240 | 17 | 39895095 | regulatory region variant | A/G | snv | 0.50 | 6 | ||
rs2305480 | 0.763 | 0.280 | 17 | 39905943 | missense variant | G/A | snv | 0.40 | 0.35 | 7 | |
rs3939286 | 0.776 | 0.360 | 9 | 6210099 | regulatory region variant | T/A;C | snv | 2 | |||
rs1342326 | 0.790 | 0.360 | 9 | 6190076 | intergenic variant | A/C | snv | 0.21 | 2 | ||
rs1837253 | 0.790 | 0.240 | 5 | 111066174 | upstream gene variant | T/C | snv | 0.72 | 2 | ||
rs2290400 | 0.790 | 0.360 | 17 | 39909987 | intron variant | T/C | snv | 0.48 | 6 | ||
rs4794820 | 0.790 | 0.160 | 17 | 39933091 | intron variant | A/G;T | snv | 3 | |||
rs8076131 | 0.790 | 0.200 | 17 | 39924659 | intron variant | G/A;C | snv | 3 | |||
rs9303277 | 0.790 | 0.240 | 17 | 39820216 | intron variant | C/T | snv | 0.52 | 4 | ||
rs12603332 | 0.807 | 0.200 | 17 | 39926554 | 5 prime UTR variant | T/C | snv | 0.49 | 3 | ||
rs1464510 | 0.807 | 0.280 | 3 | 188394766 | intron variant | C/A;T | snv | 7 | |||
rs928413 | 0.807 | 0.120 | 9 | 6213387 | upstream gene variant | G/A;C | snv | 2 | |||
rs10445308 | 0.851 | 0.240 | 17 | 39781794 | intron variant | C/T | snv | 0.38 | 3 | ||
rs11557467 | 0.851 | 0.200 | 17 | 39872381 | missense variant | G/T | snv | 0.45 | 0.45 | 4 | |
rs204993 | 0.851 | 0.240 | 6 | 32187804 | intron variant | A/G | snv | 0.24 | 0.26 | 3 | |
rs4795405 | 0.851 | 0.160 | 17 | 39932164 | intron variant | T/A;C | snv | 3 | |||
rs1888909 | 0.882 | 0.200 | 9 | 6197392 | downstream gene variant | T/A;C | snv | 2 | |||
rs2305479 | 0.882 | 0.160 | 17 | 39905964 | missense variant | C/T | snv | 0.43 | 0.39 | 4 | |
rs7130588 | 0.882 | 0.200 | 11 | 76559639 | regulatory region variant | A/G | snv | 0.29 | 3 | ||
rs7219923 | 0.882 | 0.160 | 17 | 39918265 | non coding transcript exon variant | C/T | snv | 0.52 | 4 | ||
rs8069176 | 0.882 | 0.080 | 17 | 39900944 | downstream gene variant | G/A;T | snv | 3 |