Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11065979 | 0.851 | 0.200 | 12 | 111621753 | intergenic variant | C/T | snv | 0.30 | 12 | ||
rs6063514 | 0.776 | 0.080 | 20 | 50438781 | intergenic variant | C/T | snv | 0.42 | 11 | ||
rs77542162 | 1.000 | 0.040 | 17 | 69085137 | missense variant | A/G | snv | 9.3E-03 | 1.0E-02 | 10 | |
rs11221332 | 0.763 | 0.280 | 11 | 128511079 | intron variant | C/A;T | snv | 8 | |||
rs2571445 | 0.925 | 0.080 | 2 | 217818431 | missense variant | A/G;T | snv | 0.62 | 8 | ||
rs17030613 | 1 | 112648185 | intron variant | A/C | snv | 0.19 | 6 | ||||
rs72681869 | 14 | 50188639 | missense variant | G/A;C | snv | 4.0E-06; 4.1E-03 | 6 | ||||
rs8176743 | 1.000 | 0.040 | 9 | 133256028 | missense variant | C/T | snv | 0.12 | 0.11 | 5 | |
rs72755233 | 1.000 | 0.080 | 15 | 100152748 | missense variant | G/A;T | snv | 7.1E-02; 3.2E-05 | 5 | ||
rs10774624 | 0.882 | 0.160 | 12 | 111395984 | intron variant | G/A | snv | 0.67 | 5 | ||
rs113542380 | 2 | 43237679 | intron variant | G/A | snv | 4.7E-02 | 5 | ||||
rs28383314 | 0.925 | 0.160 | 6 | 32619436 | regulatory region variant | T/C | snv | 0.61 | 4 | ||
rs8176747 | 9 | 133255928 | missense variant | C/A;G | snv | 4.1E-06; 0.12 | 4 | ||||
rs7759938 | 0.925 | 0.120 | 6 | 104931079 | intron variant | C/T | snv | 0.62 | 4 | ||
rs1042602 | 0.925 | 0.080 | 11 | 89178528 | missense variant | C/A | snv | 0.25 | 0.24 | 4 | |
rs10036789 | 1.000 | 0.080 | 5 | 72400091 | regulatory region variant | C/A;G | snv | 3 | |||
rs17752199 | 0.925 | 0.040 | 6 | 51542050 | upstream gene variant | A/C;G;T | snv | 3 | |||
rs4656461 | 0.827 | 0.040 | 1 | 165717968 | TF binding site variant | G/A | snv | 0.85 | 3 | ||
rs6478746 | 0.925 | 0.040 | 9 | 126605119 | intron variant | G/A | snv | 0.72 | 3 | ||
rs9853115 | 0.925 | 0.040 | 3 | 186413811 | intergenic variant | T/A;G | snv | 0.51 | 3 | ||
rs2305013 | 11 | 120469351 | missense variant | A/G;T | snv | 6.2E-02 | 4.2E-02 | 3 | |||
rs72766630 | 9 | 134061669 | intron variant | G/A;T | snv | 3 | |||||
rs1591805 | 1.000 | 0.040 | 6 | 126395918 | intron variant | A/G | snv | 0.47 | 3 | ||
rs4608502 | 2 | 227269439 | intron variant | T/A;C | snv | 3 | |||||
rs9608740 | 22 | 29224336 | intron variant | A/C;G;T | snv | 3 |