Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3916965 | 0.882 | 0.040 | 13 | 105451011 | intergenic variant | C/T | snv | 0.31 | 4 | ||
rs1935057 | 1.000 | 0.040 | 13 | 105458997 | upstream gene variant | G/A | snv | 0.51 | 1 | ||
rs3916967 | 0.882 | 0.040 | 13 | 105464999 | intron variant | T/C | snv | 0.32 | 3 | ||
rs2391191 | 0.807 | 0.080 | 13 | 105467097 | missense variant | G/A | snv | 0.40 | 0.32 | 7 | |
rs1046943 | 1.000 | 0.040 | 6 | 109462738 | 3 prime UTR variant | A/G | snv | 0.52 | 3 | ||
rs6318 | 0.623 | 0.520 | X | 114731326 | missense variant | C/G;T | snv | 42 | |||
rs1801133 | 0.472 | 0.880 | 1 | 11796321 | missense variant | G/A | snv | 0.31 | 0.27 | 174 | |
rs1200746244 | 0.807 | 0.080 | 1 | 11801287 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 11 | |
rs2230912 | 0.752 | 0.280 | 12 | 121184393 | missense variant | A/G | snv | 0.13 | 0.12 | 16 | |
rs781140785 | 0.925 | 0.040 | 7 | 150952801 | missense variant | C/T | snv | 1.2E-05 | 4.2E-05 | 2 | |
rs2619522 | 0.827 | 0.080 | 6 | 15653418 | intron variant | A/C | snv | 0.26 | 6 | ||
rs953038635 | 0.590 | 0.800 | 6 | 159692720 | missense variant | G/A;T | snv | 8.0E-06 | 51 | ||
rs2197414 | 1.000 | 0.040 | 5 | 161681878 | intron variant | G/A;C | snv | 1 | |||
rs4921195 | 1.000 | 0.040 | 5 | 161684582 | intron variant | C/A;T | snv | 1 | |||
rs13188991 | 1.000 | 0.040 | 5 | 161685998 | synonymous variant | G/A;C | snv | 0.19 | 0.18 | 1 | |
rs11956731 | 1.000 | 0.040 | 5 | 161700816 | intron variant | C/A;T | snv | 1 | |||
rs78247304 | 0.925 | 0.040 | 2 | 162446391 | missense variant | C/T | snv | 7.6E-05 | 6.4E-04 | 2 | |
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 | ||
rs5326 | 0.851 | 0.160 | 5 | 175443193 | 5 prime UTR variant | C/T | snv | 0.15 | 6 | ||
rs7619173 | 1.000 | 0.040 | 3 | 181279171 | intron variant | C/T | snv | 0.49 | 1 | ||
rs4680 | 0.442 | 0.920 | 22 | 19963748 | missense variant | G/A | snv | 0.46 | 0.44 | 249 | |
rs165599 | 0.677 | 0.280 | 22 | 19969258 | 3 prime UTR variant | G/A | snv | 0.56 | 27 | ||
rs11636988 | 1.000 | 0.040 | 15 | 26577667 | intron variant | G/A | snv | 0.43 | 1 | ||
rs8024256 | 1.000 | 0.040 | 15 | 26584374 | intron variant | A/G | snv | 0.61 | 1 |