Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3025039 | 0.576 | 0.720 | 6 | 43784799 | 3 prime UTR variant | C/T | snv | 0.13 | 62 | ||
rs2736098 | 0.600 | 0.600 | 5 | 1293971 | synonymous variant | C/T | snv | 0.29 | 0.22 | 48 | |
rs12917 | 0.605 | 0.480 | 10 | 129708019 | missense variant | C/T | snv | 0.14 | 0.14 | 45 | |
rs1057520009 | 0.790 | 0.200 | 2 | 61492337 | missense variant | C/T | snv | 4.4E-06 | 14 | ||
rs2231137 | 0.752 | 0.400 | 4 | 88139962 | missense variant | C/T | snv | 0.11 | 7.4E-02 | 13 | |
rs907715 | 0.752 | 0.520 | 4 | 122613898 | intron variant | C/T | snv | 0.35 | 11 | ||
rs806321 | 0.851 | 0.160 | 13 | 50267187 | intron variant | C/T | snv | 0.47 | 4 | ||
rs41289586 | 0.882 | 0.160 | 3 | 43577066 | missense variant | C/T | snv | 1.8E-02 | 1.9E-02 | 3 | |
rs13255292 | 0.925 | 0.120 | 8 | 128064327 | intron variant | C/T | snv | 0.24 | 2 | ||
rs2070770 | 0.925 | 0.120 | 11 | 60463058 | synonymous variant | C/T | snv | 7.1E-02 | 5.4E-02 | 2 | |
rs79480871 | 0.925 | 0.160 | 2 | 24471603 | intergenic variant | C/T | snv | 9.3E-02 | 2 | ||
rs121913377 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 480 | |||
rs1801133 | 0.472 | 0.880 | 1 | 11796321 | missense variant | G/A | snv | 0.31 | 0.27 | 174 | |
rs1800629 | 0.472 | 0.920 | 6 | 31575254 | upstream gene variant | G/A | snv | 0.12 | 0.14 | 169 | |
rs1799782 | 0.474 | 0.800 | 19 | 43553422 | missense variant | G/A | snv | 9.5E-02 | 7.0E-02 | 151 | |
rs745738344 | 0.653 | 0.600 | 6 | 31576786 | synonymous variant | G/A | snv | 1.6E-05 | 1.4E-05 | 28 | |
rs1883112 | 0.851 | 0.200 | 22 | 36860804 | intron variant | G/A | snv | 0.39 | 4 | ||
rs1323292 | 0.882 | 0.160 | 1 | 192571891 | intron variant | G/A | snv | 0.86 | 3 | ||
rs143002189 | 1.000 | 0.120 | 6 | 137881310 | missense variant | G/A | snv | 4.3E-04 | 4.4E-04 | 3 | |
rs1390458638 | 0.925 | 0.120 | 2 | 219216441 | missense variant | G/A | snv | 4.0E-06 | 2 | ||
rs1880030 | 0.925 | 0.120 | 12 | 122046634 | intron variant | G/A | snv | 0.39 | 2 | ||
rs2681416 | 0.925 | 0.120 | 3 | 122098766 | intron variant | G/A | snv | 0.26 | 2 | ||
rs3025684 | 1.000 | 0.120 | 16 | 3745362 | splice region variant | G/A | snv | 7.7E-02 | 0.15 | 2 | |
rs777500092 | 1.000 | 0.120 | 2 | 25246231 | missense variant | G/A | snv | 8.0E-06 | 2 | ||
rs2228479 | 0.763 | 0.280 | 16 | 89919532 | missense variant | G/A;C | snv | 7.8E-02; 4.0E-06 | 11 |