Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs150924946 | 0.882 | 0.120 | 1 | 156135271 | missense variant | A/G | snv | 4.8E-04 | 1.6E-04 | 5 | |
rs1559279177 | 0.851 | 0.160 | 1 | 146018661 | frameshift variant | G/- | del | 5 | |||
rs1967017 | 0.882 | 0.160 | 1 | 145711421 | upstream gene variant | A/G | snv | 0.43 | 5 | ||
rs2275558 | 0.882 | 0.200 | 1 | 164559883 | missense variant | G/A | snv | 0.30 | 0.19 | 5 | |
rs3789678 | 1.000 | 0.040 | 1 | 230713736 | intron variant | C/T | snv | 0.15 | 5 | ||
rs60662302 | 0.882 | 0.200 | 1 | 156138593 | missense variant | G/A | snv | 2.1E-04 | 7.7E-04 | 5 | |
rs6681231 | 0.882 | 0.120 | 1 | 186690727 | intergenic variant | G/C | snv | 0.22 | 5 | ||
rs7212 | 0.851 | 0.120 | 1 | 145992816 | 3 prime UTR variant | G/C | snv | 0.16 | 5 | ||
rs758564400 | 0.925 | 0.120 | 1 | 204156683 | missense variant | A/G | snv | 4.0E-06 | 5 | ||
rs10489177 | 0.925 | 0.120 | 1 | 169793666 | missense variant | T/A;G | snv | 4.1E-06; 0.19 | 4 | ||
rs1298417395 | 0.882 | 0.080 | 1 | 176206716 | missense variant | C/T | snv | 1.4E-05 | 4 | ||
rs1553769428 | 0.925 | 0.120 | 1 | 146018352 | stop gained | C/A | snv | 4 | |||
rs161810 | 0.925 | 0.120 | 1 | 7940737 | intron variant | T/C | snv | 0.13 | 4 | ||
rs7528153 | 0.925 | 0.080 | 1 | 107765105 | missense variant | T/A | snv | 0.58 | 0.64 | 4 | |
rs7533564 | 0.925 | 0.120 | 1 | 78360228 | intron variant | C/T | snv | 0.92 | 4 | ||
rs755725121 | 0.882 | 0.080 | 1 | 9716029 | missense variant | G/A | snv | 2.1E-05 | 7.0E-06 | 4 | |
rs12144939 | 0.925 | 0.080 | 1 | 196729815 | intron variant | G/A;T | snv | 3 | |||
rs17106184 | 0.925 | 0.080 | 1 | 50444313 | intron variant | G/A | snv | 8.5E-02 | 3 | ||
rs200879349 | 0.925 | 0.240 | 1 | 169468804 | missense variant | T/G | snv | 5.2E-05 | 6.3E-05 | 3 | |
rs2146727 | 0.925 | 0.080 | 1 | 167312910 | intron variant | G/A | snv | 0.56 | 3 | ||
rs2228146 | 0.925 | 0.120 | 1 | 154454574 | missense variant | G/A | snv | 1.3E-02; 4.0E-06 | 5.4E-02 | 3 | |
rs2275703 | 0.925 | 0.080 | 1 | 160195305 | intron variant | A/C | snv | 0.38 | 3 | ||
rs3767140 | 1.000 | 0.080 | 1 | 21888152 | intron variant | C/A | snv | 0.25 | 3 | ||
rs3767434 | 0.925 | 0.080 | 1 | 167401914 | intron variant | T/C | snv | 0.14 | 3 | ||
rs7539020 | 1.000 | 0.040 | 1 | 230713444 | intron variant | C/T | snv | 0.43 | 3 |