Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs5844572 | 0.752 | 0.360 | 22 | 23893562 | intron variant | -/ATTC | delins | 11 | |||
rs1032129 | 0.851 | 0.040 | 8 | 118939661 | intron variant | A/C | snv | 0.37 | 5 | ||
rs11073337 | 0.851 | 0.040 | 15 | 38555562 | intron variant | A/C | snv | 0.27 | 5 | ||
rs1199047 | 0.882 | 11 | 64350711 | intron variant | A/C | snv | 0.38 | 4 | |||
rs10892286 | 11 | 118771376 | intron variant | A/C | snv | 0.17 | 2 | ||||
rs17758761 | 1.000 | 0.080 | 17 | 55977164 | intron variant | A/C | snv | 4.1E-02 | 2 | ||
rs1801274 | 0.597 | 0.800 | 1 | 161509955 | missense variant | A/C;G | snv | 4.0E-06; 0.48 | 46 | ||
rs12720356 | 0.752 | 0.360 | 19 | 10359299 | missense variant | A/C;G | snv | 6.1E-02; 4.0E-06 | 12 | ||
rs104895271 | 0.851 | 0.240 | 12 | 6334161 | missense variant | A/C;G | snv | 1.6E-04; 4.8E-05 | 6 | ||
rs1250552 | 0.882 | 0.200 | 10 | 79298270 | intron variant | A/C;G | snv | 5 | |||
rs13010713 | 0.882 | 0.200 | 2 | 181131318 | intron variant | A/C;G | snv | 5 | |||
rs9792269 | 0.882 | 0.200 | 8 | 128252343 | intergenic variant | A/C;G | snv | 5 | |||
rs1310182 | 0.882 | 0.360 | 1 | 113830881 | intron variant | A/C;G | snv | 0.56 | 4 | ||
rs1921445 | 0.882 | 3 | 106229671 | intergenic variant | A/C;G | snv | 4 | ||||
rs2456973 | 0.925 | 0.040 | 12 | 56023144 | intron variant | A/C;G | snv | 4 | |||
rs6848139 | 1.000 | 0.040 | 4 | 122473886 | intergenic variant | A/C;G | snv | 3 | |||
rs4288027 | 4 | 122262050 | intron variant | A/C;G | snv | 0.13 | 2 | ||||
rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 490 | ||
rs10735810 | 0.662 | 0.640 | 12 | 47879112 | start lost | A/C;G;T | snv | 26 | |||
rs11145763 | 0.724 | 0.240 | 9 | 136369144 | intron variant | A/C;G;T | snv | 14 | |||
rs396991 | 0.742 | 0.480 | 1 | 161544752 | missense variant | A/C;G;T | snv | 0.33; 4.1E-06 | 14 | ||
rs391851 | 0.882 | 5 | 103342219 | intergenic variant | A/C;G;T | snv | 4 | ||||
rs8192284 | 0.724 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 19 | |||
rs179008 | 0.763 | 0.360 | X | 12885540 | missense variant | A/C;T | snv | 0.18 | 0.18 | 14 | |
rs8061370 | 0.882 | 16 | 11364614 | intron variant | A/C;T | snv | 4 |