Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1800629 | 0.472 | 0.920 | 6 | 31575254 | upstream gene variant | G/A | snv | 0.12 | 0.14 | 169 | |
rs1800795 | 0.494 | 0.840 | 7 | 22727026 | intron variant | C/G | snv | 0.71 | 140 | ||
rs1800872 | 0.495 | 0.840 | 1 | 206773062 | 5 prime UTR variant | T/G | snv | 0.69 | 119 | ||
rs1800896 | 0.507 | 0.800 | 1 | 206773552 | intron variant | T/C | snv | 0.41 | 113 | ||
rs1800871 | 0.508 | 0.800 | 1 | 206773289 | 5 prime UTR variant | A/G | snv | 0.69 | 108 | ||
rs20541 | 0.585 | 0.720 | 5 | 132660272 | missense variant | A/G | snv | 0.72 | 0.77 | 52 | |
rs2430561 | 0.590 | 0.760 | 12 | 68158742 | intron variant | T/A | snv | 0.36 | 50 | ||
rs1800890 | 0.658 | 0.400 | 1 | 206776020 | intron variant | A/T | snv | 0.32 | 29 | ||
rs2395185 | 0.724 | 0.360 | 6 | 32465390 | intron variant | G/T | snv | 0.29 | 17 | ||
rs1801177 | 0.742 | 0.240 | 8 | 19948197 | missense variant | G/A;C | snv | 1.4E-02; 2.0E-05 | 14 | ||
rs1057520009 | 0.790 | 0.200 | 2 | 61492337 | missense variant | C/T | snv | 4.4E-06 | 14 | ||
rs419598 | 0.742 | 0.280 | 2 | 113129630 | synonymous variant | T/C | snv | 0.26 | 0.21 | 13 | |
rs6903608 | 0.742 | 0.400 | 6 | 32460508 | intron variant | C/G;T | snv | 11 | |||
rs2248462 | 0.807 | 0.240 | 6 | 31479019 | downstream gene variant | G/A | snv | 0.19 | 10 | ||
rs2734986 | 0.827 | 0.160 | 6 | 29850791 | intron variant | T/C | snv | 0.10 | 5 | ||
rs27524 | 0.851 | 0.160 | 5 | 96766240 | intron variant | A/G | snv | 0.61 | 4 | ||
rs6904029 | 0.851 | 0.200 | 6 | 29975290 | non coding transcript exon variant | G/A | snv | 0.29 | 0.26 | 4 | |
rs223828 | 0.882 | 0.240 | 16 | 57413502 | intron variant | T/A;C | snv | 3 | |||
rs10813831 | 0.925 | 0.120 | 9 | 32526148 | missense variant | G/A | snv | 0.21 | 0.24 | 2 | |
rs6457715 | 0.925 | 0.120 | 6 | 33115411 | intron variant | A/G | snv | 0.35 | 2 |