Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6318 | 0.623 | 0.520 | X | 114731326 | missense variant | C/G;T | snv | 42 | |||
rs6295 | 0.645 | 0.200 | 5 | 63962738 | intron variant | C/G | snv | 0.49 | 40 | ||
rs165599 | 0.677 | 0.280 | 22 | 19969258 | 3 prime UTR variant | G/A | snv | 0.56 | 27 | ||
rs5848 | 0.708 | 0.120 | 17 | 44352876 | 3 prime UTR variant | C/T | snv | 0.41 | 17 | ||
rs956572 | 0.742 | 0.280 | 18 | 63153338 | intron variant | A/G | snv | 0.65 | 11 | ||
rs2619522 | 0.827 | 0.080 | 6 | 15653418 | intron variant | A/C | snv | 0.26 | 6 | ||
rs5326 | 0.851 | 0.160 | 5 | 175443193 | 5 prime UTR variant | C/T | snv | 0.15 | 6 | ||
rs3916965 | 0.882 | 0.040 | 13 | 105451011 | intergenic variant | C/T | snv | 0.31 | 4 | ||
rs1046943 | 1.000 | 0.040 | 6 | 109462738 | 3 prime UTR variant | A/G | snv | 0.52 | 3 | ||
rs3916967 | 0.882 | 0.040 | 13 | 105464999 | intron variant | T/C | snv | 0.32 | 3 | ||
rs11637898 | 0.925 | 0.040 | 15 | 92409620 | intron variant | G/A | snv | 0.43 | 2 | ||
rs17026688 | 1.000 | 0.040 | 3 | 30845325 | intron variant | C/T | snv | 9.3E-03 | 2 | ||
rs11001178 | 1.000 | 0.040 | 10 | 74842047 | intron variant | T/C;G | snv | 1 | |||
rs11636988 | 1.000 | 0.040 | 15 | 26577667 | intron variant | G/A | snv | 0.43 | 1 | ||
rs11956731 | 1.000 | 0.040 | 5 | 161700816 | intron variant | C/A;T | snv | 1 | |||
rs12547858 | 1.000 | 0.040 | 8 | 32629535 | intron variant | C/T | snv | 0.15 | 1 | ||
rs1475196 | 1.000 | 0.040 | 13 | 46881488 | intron variant | A/C | snv | 1.4E-03 | 1 | ||
rs17110566 | 1.000 | 0.040 | 12 | 71972867 | intron variant | G/A | snv | 3.9E-02 | 1 | ||
rs1935057 | 1.000 | 0.040 | 13 | 105458997 | upstream gene variant | G/A | snv | 0.51 | 1 | ||
rs2197414 | 1.000 | 0.040 | 5 | 161681878 | intron variant | G/A;C | snv | 1 | |||
rs2217887 | 1.000 | 0.040 | 14 | 79417482 | intron variant | T/C | snv | 0.31 | 1 | ||
rs3757933 | 1.000 | 0.040 | 8 | 32747325 | intron variant | G/A | snv | 0.23 | 1 | ||
rs3815762 | 1.000 | 0.040 | 5 | 170788816 | intron variant | T/A | snv | 0.11 | 1 | ||
rs4868029 | 1.000 | 0.040 | 5 | 170790498 | intron variant | C/T | snv | 0.36 | 1 | ||
rs4921195 | 1.000 | 0.040 | 5 | 161684582 | intron variant | C/A;T | snv | 1 |