Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10445308 | 0.851 | 0.240 | 17 | 39781794 | intron variant | C/T | snv | 0.38 | 3 | ||
rs10484561 | 0.827 | 0.160 | 6 | 32697643 | intergenic variant | T/G | snv | 0.13 | 3 | ||
rs11078925 | 0.925 | 0.160 | 17 | 39868955 | intron variant | T/C | snv | 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 | ||
rs13192471 | 0.925 | 0.160 | 6 | 32703326 | downstream gene variant | T/C | snv | 0.19 | 3 | ||
rs17293632 | 0.763 | 0.240 | 15 | 67150258 | intron variant | C/T | snv | 0.17 | 3 | ||
rs17388568 | 0.827 | 0.280 | 4 | 122408207 | intron variant | G/A | snv | 0.20 | 3 | ||
rs176095 | 0.925 | 0.160 | 6 | 32190542 | upstream gene variant | A/G | snv | 0.22 | 3 | ||
rs2523477 | 0.925 | 0.080 | 6 | 31392612 | downstream gene variant | T/C | snv | 0.10 | 3 | ||
rs2596480 | 0.925 | 0.120 | 6 | 31458208 | intron variant | C/G;T | snv | 3 | |||
rs3091307 | 0.925 | 0.160 | 5 | 132653444 | intron variant | A/G | snv | 0.34 | 3 | ||
rs3816470 | 0.925 | 0.160 | 17 | 39829548 | intron variant | A/G | snv | 0.54 | 3 | ||
rs4794820 | 0.790 | 0.160 | 17 | 39933091 | intron variant | A/G;T | snv | 3 | |||
rs4795400 | 0.925 | 0.080 | 17 | 39910767 | intron variant | C/T | snv | 0.36 | 3 | ||
rs4795405 | 0.851 | 0.160 | 17 | 39932164 | intron variant | T/A;C | snv | 3 | |||
rs6906021 | 0.827 | 0.320 | 6 | 32658534 | upstream gene variant | T/C | snv | 0.47 | 3 | ||
rs7130588 | 0.882 | 0.200 | 11 | 76559639 | regulatory region variant | A/G | snv | 0.29 | 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 | ||
rs8069176 | 0.882 | 0.080 | 17 | 39900944 | downstream gene variant | G/A;T | snv | 3 |