Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs259919 | 0.882 | 0.080 | 6 | 30057726 | intron variant | G/A | snv | 0.25 | 6 | ||
rs174577 | 1.000 | 0.080 | 11 | 61837342 | intron variant | C/A | snv | 0.38 | 5 | ||
rs1062980 | 0.827 | 0.080 | 15 | 78500185 | 3 prime UTR variant | T/C | snv | 0.39 | 4 | ||
rs11638372 | 0.925 | 0.080 | 15 | 78691217 | intron variant | C/A;G;T | snv | 0.28 | 3 | ||
rs12441998 | 0.925 | 0.080 | 15 | 78637030 | intron variant | G/A | snv | 0.63 | 3 | ||
rs12594247 | 0.925 | 0.080 | 15 | 78654291 | intron variant | C/T | snv | 0.14 | 3 | ||
rs12910984 | 0.827 | 0.080 | 15 | 78599285 | intron variant | G/A;C;T | snv | 3 | |||
rs1316971 | 0.925 | 0.080 | 15 | 78638168 | intron variant | A/G;T | snv | 0.62 | 3 | ||
rs1394371 | 0.925 | 0.080 | 15 | 78432127 | intergenic variant | C/T | snv | 0.22 | 3 | ||
rs174534 | 1.000 | 0.080 | 11 | 61781986 | non coding transcript exon variant | A/G | snv | 0.28 | 3 | ||
rs17487514 | 0.925 | 0.080 | 15 | 78661443 | non coding transcript exon variant | C/T | snv | 0.19 | 3 | ||
rs2036527 | 0.851 | 0.080 | 15 | 78559273 | regulatory region variant | G/A | snv | 0.29 | 3 | ||
rs2036534 | 0.827 | 0.080 | 15 | 78534606 | 3 prime UTR variant | T/C | snv | 0.26 | 3 | ||
rs2656069 | 0.882 | 0.080 | 15 | 78453365 | intron variant | C/G;T | snv | 3 | |||
rs3813565 | 0.851 | 0.080 | 15 | 78727268 | splice region variant | G/A;T | snv | 3 | |||
rs4887053 | 0.925 | 0.080 | 15 | 78420357 | regulatory region variant | A/C;T | snv | 3 | |||
rs6495309 | 0.807 | 0.080 | 15 | 78622903 | upstream gene variant | C/A;T | snv | 3 | |||
rs6495314 | 0.925 | 0.080 | 15 | 78668187 | intron variant | A/C | snv | 0.35 | 3 | ||
rs8038920 | 0.925 | 0.080 | 15 | 78682203 | intron variant | A/G | snv | 0.62 | 3 | ||
rs938682 | 0.851 | 0.080 | 15 | 78604205 | intron variant | G/A | snv | 0.72 | 3 | ||
rs10519198 | 0.925 | 0.080 | 15 | 78450412 | intron variant | C/A;G | snv | 2 | |||
rs11072793 | 1.000 | 0.080 | 15 | 78714100 | intron variant | G/A | snv | 0.58 | 2 | ||
rs1489759 | 0.882 | 0.080 | 4 | 144553321 | intron variant | A/G | snv | 0.43 | 2 | ||
rs1996371 | 1.000 | 0.080 | 15 | 78664464 | intron variant | T/C | snv | 0.28 | 2 | ||
rs2256543 | 0.925 | 0.080 | 6 | 29970056 | downstream gene variant | T/C | snv | 0.59 | 2 |