Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10811474 | 0.742 | 0.240 | 9 | 21114238 | intergenic variant | A/G | snv | 0.44 | 11 | ||
rs12826786 | 0.683 | 0.480 | 12 | 53961717 | upstream gene variant | C/T | snv | 0.38 | 26 | ||
rs2069514 | 0.807 | 0.160 | 15 | 74745879 | upstream gene variant | G/A | snv | 0.13 | 9 | ||
rs2736108 | 0.807 | 0.160 | 5 | 1297373 | upstream gene variant | C/T | snv | 0.24 | 6 | ||
rs3094054 | 0.807 | 0.280 | 6 | 30365728 | upstream gene variant | G/A;T | snv | 6 | |||
rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
rs1128503 | 0.564 | 0.760 | 7 | 87550285 | synonymous variant | A/G | snv | 0.54 | 0.63 | 64 | |
rs2032582 | 0.538 | 0.800 | 7 | 87531302 | missense variant | A/C;T | snv | 0.54; 3.8E-02 | 97 | ||
rs3132610 | 0.807 | 0.280 | 6 | 30576624 | intron variant | A/G | snv | 7.4E-02 | 6 | ||
rs2231142 | 0.583 | 0.680 | 4 | 88131171 | missense variant | G/C;T | snv | 4.0E-06; 0.12 | 56 | ||
rs1682111 | 0.742 | 0.240 | 2 | 54200842 | intron variant | A/T | snv | 0.56 | 13 | ||
rs2241766 | 0.608 | 0.720 | 3 | 186853103 | synonymous variant | T/C;G | snv | 8.0E-06; 0.13 | 48 | ||
rs2070600 | 0.561 | 0.760 | 6 | 32183666 | missense variant | C/T | snv | 5.3E-02 | 3.6E-02 | 82 | |
rs2066853 | 0.653 | 0.600 | 7 | 17339486 | missense variant | G/A | snv | 0.15 | 0.22 | 34 | |
rs121434592 | 0.595 | 0.640 | 14 | 104780214 | missense variant | C/T | snv | 4.0E-06 | 54 | ||
rs1130409 | 0.555 | 0.720 | 14 | 20456995 | missense variant | T/A;C;G | snv | 4.0E-06; 4.0E-06; 0.42 | 72 | ||
rs3136820 | 0.776 | 0.200 | 14 | 20456995 | missense variant | T/A;C;G | snv | 8 | |||
rs3136817 | 0.732 | 0.280 | 14 | 20456275 | intron variant | T/C | snv | 0.23 | 12 | ||
rs3816358 | 0.827 | 0.120 | 11 | 13369925 | intron variant | C/A;T | snv | 5 | |||
rs3816360 | 0.807 | 0.120 | 11 | 13346203 | intron variant | T/C | snv | 0.58 | 6 | ||
rs200847762 | 0.790 | 0.160 | 6 | 32129371 | missense variant | G/A | snv | 2.7E-04 | 1.4E-05 | 7 | |
rs10514231 | 0.807 | 0.160 | 5 | 82011593 | intron variant | C/T | snv | 0.56 | 6 | ||
rs1864182 | 0.827 | 0.120 | 5 | 82253421 | missense variant | C/A;G | snv | 0.59 | 0.47 | 6 | |
rs1801516 | 0.627 | 0.400 | 11 | 108304735 | missense variant | G/A | snv | 0.11 | 0.11 | 39 | |
rs624366 | 0.827 | 0.120 | 11 | 108283370 | intron variant | G/C | snv | 0.52 | 6 |