Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2305480 | 0.763 | 0.280 | 17 | 39905943 | missense variant | G/A | snv | 0.40 | 0.35 | 7 | |
rs2872507 | 0.752 | 0.360 | 17 | 39884510 | intergenic variant | G/A;T | snv | 7 | |||
rs2290400 | 0.790 | 0.360 | 17 | 39909987 | intron variant | T/C | snv | 0.48 | 6 | ||
rs8067378 | 0.752 | 0.240 | 17 | 39895095 | regulatory region variant | A/G | snv | 0.50 | 6 | ||
rs11557467 | 0.851 | 0.200 | 17 | 39872381 | missense variant | G/T | snv | 0.45 | 0.45 | 4 | |
rs2305479 | 0.882 | 0.160 | 17 | 39905964 | missense variant | C/T | snv | 0.43 | 0.39 | 4 | |
rs7219923 | 0.882 | 0.160 | 17 | 39918265 | non coding transcript exon variant | C/T | snv | 0.52 | 4 | ||
rs9303277 | 0.790 | 0.240 | 17 | 39820216 | intron variant | C/T | snv | 0.52 | 4 | ||
rs9303281 | 0.882 | 0.160 | 17 | 39917793 | non coding transcript exon variant | G/A | snv | 0.50 | 4 | ||
rs1008723 | 0.925 | 0.160 | 17 | 39910014 | intron variant | G/C;T | snv | 3 | |||
rs10445308 | 0.851 | 0.240 | 17 | 39781794 | intron variant | C/T | snv | 0.38 | 3 | ||
rs11078925 | 0.925 | 0.160 | 17 | 39868955 | intron variant | T/C | snv | 0.36 | 3 | ||
rs11557466 | 0.925 | 0.160 | 17 | 39868373 | synonymous variant | C/T | snv | 0.40 | 0.36 | 3 | |
rs11870965 | 0.925 | 0.160 | 17 | 39873952 | intron variant | T/A | snv | 0.40 | 3 | ||
rs12232497 | 0.701 | 0.360 | 17 | 39883866 | intergenic variant | T/C | snv | 0.35 | 3 | ||
rs12603332 | 0.807 | 0.200 | 17 | 39926554 | 5 prime UTR variant | T/C | snv | 0.49 | 3 | ||
rs12936231 | 0.925 | 0.160 | 17 | 39872867 | intron variant | C/G;T | snv | 3 | |||
rs12950743 | 0.925 | 0.160 | 17 | 39892980 | intergenic variant | T/C | snv | 0.45 | 3 | ||
rs3816470 | 0.925 | 0.160 | 17 | 39829548 | intron variant | A/G | snv | 0.54 | 3 | ||
rs7216389 | 0.732 | 0.440 | 17 | 39913696 | intron variant | C/T | snv | 0.60 | 3 | ||
rs7224129 | 0.925 | 0.160 | 17 | 39919173 | non coding transcript exon variant | G/A | snv | 0.52 | 3 | ||
rs7359623 | 0.925 | 0.160 | 17 | 39893336 | intergenic variant | C/T | snv | 0.44 | 3 | ||
rs869402 | 0.925 | 0.160 | 17 | 39911790 | intron variant | T/A;C | snv | 3 | |||
rs9901146 | 0.882 | 0.160 | 17 | 39887090 | intergenic variant | G/A | snv | 0.45 | 3 | ||
rs9907088 | 0.925 | 0.160 | 17 | 39878863 | downstream gene variant | G/A | snv | 0.39 | 3 |