Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1572982 | 0.827 | 0.200 | 6 | 26094139 | intron variant | G/A;T | snv | 0.52; 8.0E-06 | 7 | ||
rs12483959 | 1.000 | 22 | 43930116 | intron variant | G/A;C;T | snv | 4 | ||||
rs903361 | 0.882 | 0.160 | 1 | 203122146 | intron variant | G/A;C | snv | 4 | |||
rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 262 | |
rs2281135 | 0.851 | 0.160 | 22 | 43936690 | intron variant | G/A | snv | 0.19 | 10 | ||
rs9940128 | 0.851 | 0.120 | 16 | 53766842 | intron variant | G/A | snv | 0.42 | 10 | ||
rs3480 | 0.807 | 0.160 | 1 | 32862564 | 3 prime UTR variant | G/A | snv | 0.56 | 8 | ||
rs4823173 | 0.827 | 0.200 | 22 | 43932850 | intron variant | G/A | snv | 0.24 | 0.18 | 8 | |
rs2143571 | 0.827 | 0.080 | 22 | 43995806 | intron variant | G/A | snv | 0.25 | 5 | ||
rs951599607 | 0.925 | 0.040 | 3 | 12434028 | missense variant | G/A | snv | 4 | |||
rs1883349 | 1.000 | 22 | 43936063 | intron variant | G/A | snv | 0.19 | 1 | |||
rs2281298 | 1.000 | 22 | 43995354 | intron variant | G/A | snv | 0.21 | 1 | |||
rs926633 | 1.000 | 22 | 43941653 | intron variant | G/A | snv | 0.20 | 1 | |||
rs2070600 | 0.561 | 0.760 | 6 | 32183666 | missense variant | C/T | snv | 5.3E-02 | 3.6E-02 | 82 | |
rs58542926 | 0.630 | 0.440 | 19 | 19268740 | missense variant | C/T | snv | 6.5E-02 | 5.8E-02 | 42 | |
rs8192678 | 0.667 | 0.440 | 4 | 23814039 | missense variant | C/T | snv | 0.31 | 0.26 | 28 | |
rs694539 | 0.776 | 0.200 | 11 | 114262697 | intron variant | C/T | snv | 0.21 | 10 | ||
rs738408 | 0.925 | 0.120 | 22 | 43928850 | synonymous variant | C/T | snv | 0.28 | 0.22 | 10 | |
rs7946 | 0.851 | 0.160 | 17 | 17506246 | missense variant | C/T | snv | 0.59 | 0.59 | 6 | |
rs12447924 | 1.000 | 16 | 56960280 | upstream gene variant | C/T | snv | 0.76 | 3 | |||
rs2235776 | 0.925 | 0.040 | 22 | 43982119 | intron variant | C/T | snv | 0.24 | 3 | ||
rs72563732 | 0.882 | 0.040 | 3 | 186854563 | synonymous variant | C/T | snv | 6.4E-05 | 2.6E-04 | 3 | |
rs738491 | 0.882 | 0.040 | 22 | 43958231 | intron variant | C/T | snv | 0.34 | 3 | ||
rs2073080 | 0.925 | 0.040 | 22 | 43998522 | intron variant | C/T | snv | 0.20 | 2 | ||
rs6006473 | 0.925 | 0.040 | 22 | 43997195 | intron variant | C/T | snv | 0.47 | 2 |