Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1896286 | 0.925 | 0.080 | 2 | 203967715 | intergenic variant | G/T | snv | 0.49 | 2 | ||
rs4274624 | 0.925 | 0.080 | 2 | 191093930 | intron variant | C/G;T | snv | 2 | |||
rs13422767 | 0.882 | 0.120 | 2 | 162243749 | intron variant | G/A | snv | 0.14 | 3 | ||
rs6473 | 0.851 | 0.160 | 6 | 32041127 | missense variant | G/A;C | snv | 3.7E-04; 8.4E-06 | 4 | ||
rs10931481 | 0.827 | 0.240 | 2 | 191090126 | intron variant | G/A | snv | 0.66 | 5 | ||
rs3757247 | 0.827 | 0.320 | 6 | 90247744 | intron variant | C/T | snv | 0.38 | 5 | ||
rs3136534 | 0.807 | 0.240 | 4 | 122448621 | downstream gene variant | T/G | snv | 0.29 | 6 | ||
rs3827440 | 0.851 | 0.120 | X | 79171491 | missense variant | T/A;C | snv | 5.5E-06; 0.51 | 6 | ||
rs231726 | 0.790 | 0.200 | 2 | 203876143 | downstream gene variant | C/T | snv | 0.36 | 7 | ||
rs3118470 | 0.752 | 0.360 | 10 | 6059750 | intron variant | T/A;C | snv | 10 | |||
rs12150220 | 0.724 | 0.360 | 17 | 5582047 | missense variant | A/T | snv | 0.37 | 0.33 | 14 | |
rs2111485 | 0.724 | 0.280 | 2 | 162254026 | regulatory region variant | A/G | snv | 0.46 | 17 | ||
rs6822844 | 0.689 | 0.520 | 4 | 122588266 | regulatory region variant | G/T | snv | 0.10 | 20 | ||
rs763361 | 0.689 | 0.520 | 18 | 69864406 | missense variant | T/A;C | snv | 4.0E-06; 0.52 | 21 | ||
rs2104286 | 0.662 | 0.440 | 10 | 6057082 | intron variant | T/C | snv | 0.18 | 25 | ||
rs1990760 | 0.672 | 0.480 | 2 | 162267541 | missense variant | C/T | snv | 0.50 | 0.45 | 33 | |
rs231775 | 0.504 | 0.720 | 2 | 203867991 | missense variant | A/G;T | snv | 0.42; 4.0E-06 | 115 | ||
rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 121 |