Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1321311 | 0.742 | 0.160 | 6 | 36655123 | regulatory region variant | C/A | snv | 0.28 | 15 | ||
rs174577 | 1.000 | 0.080 | 11 | 61837342 | intron variant | C/A | snv | 0.38 | 13 | ||
rs6795970 | 0.807 | 0.200 | 3 | 38725184 | missense variant | A/G | snv | 0.65 | 0.70 | 13 | |
rs9470361 | 0.776 | 0.080 | 6 | 36655602 | regulatory region variant | G/A;T | snv | 12 | |||
rs17608766 | 1.000 | 0.040 | 17 | 46935905 | 3 prime UTR variant | T/C | snv | 9.2E-02 | 8 | ||
rs3825214 | 0.851 | 0.080 | 12 | 114357638 | intron variant | G/A | snv | 0.77 | 8 | ||
rs6801957 | 1.000 | 0.080 | 3 | 38725824 | intron variant | T/C | snv | 0.67 | 7 | ||
rs11708996 | 0.925 | 0.120 | 3 | 38592432 | intron variant | G/C | snv | 0.11 | 6 | ||
rs11153730 | 6 | 118346359 | intergenic variant | T/C | snv | 0.40 | 4 | ||||
rs11710077 | 3 | 38616408 | intron variant | A/T | snv | 0.17 | 3 | ||||
rs13165478 | 5 | 154489480 | upstream gene variant | G/A | snv | 0.41 | 3 | ||||
rs2025096 | 20 | 34952197 | 5 prime UTR variant | G/A | snv | 0.19 | 3 | ||||
rs4642101 | 1.000 | 0.080 | 3 | 12800724 | intron variant | T/G | snv | 0.63 | 3 | ||
rs883079 | 1.000 | 0.080 | 12 | 114355435 | 3 prime UTR variant | C/G;T | snv | 1.8E-05; 0.61 | 3 | ||
rs9912468 | 17 | 66322239 | intron variant | G/A;C | snv | 3 | |||||
rs10850409 | 12 | 114943935 | intergenic variant | G/A | snv | 0.27 | 2 | ||||
rs11848785 | 14 | 71590638 | intron variant | G/A | snv | 0.82 | 2 | ||||
rs12036340 | 1 | 162045950 | intergenic variant | A/G | snv | 0.24 | 2 | ||||
rs13195040 | 1.000 | 0.040 | 6 | 27446145 | downstream gene variant | A/G | snv | 9.0E-02 | 2 | ||
rs1362212 | 7 | 35265695 | intergenic variant | G/A | snv | 0.11 | 2 | ||||
rs17020136 | 2 | 37020872 | intron variant | T/C | snv | 0.24 | 0.18 | 2 | |||
rs1733724 | 10 | 52464217 | intron variant | A/G | snv | 0.82 | 2 | ||||
rs17391905 | 1 | 51080468 | intergenic variant | T/G | snv | 3.7E-02 | 2 | ||||
rs1886512 | 13 | 73946049 | intron variant | T/A | snv | 0.40 | 2 | ||||
rs2242285 | 3 | 66381178 | intron variant | A/C;G | snv | 2 |