Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs267607555 | 0.807 | 0.280 | 1 | 156136009 | missense variant | C/T | snv | 7.0E-06 | 6 | ||
rs267606879 | 0.925 | 0.080 | 14 | 104703428 | missense variant | G/A | snv | 7.0E-06 | 2 | ||
rs1283740147 | 1.000 | 0.080 | 19 | 45777777 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 1 | |
rs121908415 | 0.925 | 0.080 | 19 | 38710286 | missense variant | A/G | snv | 7.0E-06 | 2 | ||
rs754313620 | 0.925 | 0.080 | 14 | 104714452 | missense variant | T/C;G | snv | 7.0E-06 | 2 | ||
rs761613959 | 0.851 | 0.080 | 1 | 155187356 | stop gained | G/A | snv | 3.2E-05 | 7.0E-06 | 4 | |
rs779430565 | 0.882 | 0.080 | 11 | 101504316 | missense variant | T/A | snv | 1.2E-05 | 1.4E-05 | 3 | |
rs140511594 | 0.742 | 0.360 | 2 | 165941111 | missense variant | G/A | snv | 1.3E-04 | 1.1E-04 | 13 | |
rs119473033 | 0.827 | 0.320 | 2 | 216478216 | stop gained | G/T | snv | 8.0E-05 | 1.3E-04 | 11 | |
rs149117087 | 1.000 | 0.080 | 2 | 227022069 | missense variant | T/A | snv | 8.5E-04 | 2.0E-04 | 1 | |
rs74315342 | 0.763 | 0.120 | 1 | 179561327 | missense variant | C/T | snv | 6.0E-04 | 5.3E-04 | 10 | |
rs2234591 | 0.925 | 0.080 | 11 | 32399873 | intron variant | T/C | snv | 1.4E-03 | 2 | ||
rs114896482 | 0.882 | 0.080 | 19 | 35842487 | missense variant | G/A | snv | 2.3E-03 | 1.5E-03 | 3 | |
rs74315344 | 0.851 | 0.080 | 1 | 179575806 | missense variant | G/A | snv | 2.8E-03 | 4.2E-03 | 4 | |
rs112545413 | 0.925 | 0.080 | 19 | 38717102 | missense variant | G/A | snv | 1.2E-02 | 9.6E-03 | 2 | |
rs61747728 | 0.701 | 0.240 | 1 | 179557079 | missense variant | C/T | snv | 3.0E-02 | 2.8E-02 | 20 | |
rs5742909 | 0.614 | 0.680 | 2 | 203867624 | upstream gene variant | C/T | snv | 6.7E-02 | 40 | ||
rs3802829 | 0.925 | 0.080 | 11 | 101583461 | missense variant | G/A | snv | 8.2E-02 | 7.0E-02 | 2 | |
rs4806213 | 1.000 | 0.080 | 19 | 35831699 | missense variant | T/C | snv | 9.7E-02 | 0.11 | 1 | |
rs6508 | 0.882 | 0.160 | 11 | 32438918 | non coding transcript exon variant | G/A | snv | 8.3E-02 | 0.16 | 3 | |
rs2071327 | 1.000 | 0.080 | 19 | 35831368 | synonymous variant | C/T | snv | 0.40 | 0.32 | 1 | |
rs1799937 | 0.882 | 0.160 | 11 | 32389228 | intron variant | A/G | snv | 0.35 | 0.35 | 3 | |
rs2301254 | 0.882 | 0.160 | 11 | 32436129 | intron variant | A/G | snv | 0.48 | 3 | ||
rs699 | 0.501 | 0.800 | 1 | 230710048 | missense variant | A/G | snv | 0.55 | 0.58 | 134 | |
rs2239785 | 0.827 | 0.240 | 22 | 36265284 | missense variant | G/A | snv | 0.79 | 0.68 | 5 |