Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12826786 | 0.683 | 0.480 | 12 | 53961717 | upstream gene variant | C/T | snv | 0.38 | 26 | ||
rs35753505 | 0.827 | 0.080 | 8 | 31616625 | intergenic variant | T/A;C | snv | 6 | |||
rs2388334 | 0.882 | 0.040 | 6 | 98143746 | intron variant | A/G | snv | 0.39 | 5 | ||
rs4307059 | 0.882 | 0.080 | 5 | 25967594 | intron variant | T/A;C | snv | 5 | |||
rs11787216 | 1.000 | 0.040 | 8 | 141605122 | intron variant | C/T | snv | 0.26 | 2 | ||
rs13000344 | 0.925 | 0.040 | 2 | 63062599 | downstream gene variant | T/G | snv | 0.11 | 2 | ||
rs13294439 | 1.000 | 0.040 | 9 | 23358877 | intron variant | A/C | snv | 0.32 | 2 | ||
rs34808376 | 0.925 | 0.040 | 7 | 155456016 | intron variant | -/GC | delins | 2 | |||
rs6150410 | 0.925 | 0.040 | 7 | 155454910 | intron variant | CGCATCCCC/-;CGCATCCCCCGCATCCCC | delins | 0.28 | 2 | ||
rs194085 | 1.000 | 0.040 | 5 | 9591303 | intergenic variant | A/G | snv | 0.15 | 1 | ||
rs73598374 | 0.790 | 0.280 | 20 | 44651586 | missense variant | C/A;G;T | snv | 7.1E-06; 6.2E-02 | 8 | ||
rs379863 | 1.000 | 0.040 | 20 | 44632053 | intron variant | C/T | snv | 0.73 | 1 | ||
rs6551665 | 0.882 | 0.040 | 4 | 61873823 | intron variant | G/A | snv | 0.59 | 4 | ||
rs2236624 | 0.925 | 0.200 | 22 | 24440056 | intron variant | T/C | snv | 0.80 | 2 | ||
rs765619798 | 0.925 | 0.040 | 8 | 26864720 | missense variant | C/A;T | snv | 2 | |||
rs370956755 | 0.925 | 0.040 | 2 | 96115984 | missense variant | C/A;T | snv | 4.0E-06; 1.6E-05 | 2 | ||
rs1800497 | 0.620 | 0.400 | 11 | 113400106 | missense variant | G/A | snv | 0.26 | 0.26 | 56 | |
rs766483232 | 1.000 | 0.040 | 15 | 29114003 | missense variant | A/C;G | snv | 4.0E-06; 3.6E-04 | 1 | ||
rs465899 | 0.882 | 0.160 | 5 | 112841474 | synonymous variant | G/A | snv | 0.65 | 0.60 | 3 | |
rs1804197 | 1.000 | 0.040 | 5 | 112844212 | 3 prime UTR variant | C/A | snv | 7.2E-02 | 2 | ||
rs4446909 | 0.925 | 0.040 | Y | 1614890 | upstream gene variant | G/A | snv | 2 | |||
rs5989681 | 1.000 | 0.040 | Y | 1614999 | upstream gene variant | G/A;C | snv | 1 | |||
rs35424709 | 0.925 | 0.040 | 3 | 193454190 | missense variant | T/A | snv | 8.6E-02 | 7.8E-02 | 2 | |
rs2278556 | 0.925 | 0.040 | 3 | 10360419 | intron variant | G/A | snv | 0.34 | 2 | ||
rs35678 | 0.925 | 0.040 | 3 | 10338239 | missense variant | C/T | snv | 0.49 | 0.47 | 2 |