Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
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 | |||
rs12720356 | 0.752 | 0.360 | 19 | 10359299 | missense variant | A/C;G | snv | 6.1E-02; 4.0E-06 | 7 | ||
rs1801274 | 0.597 | 0.800 | 1 | 161509955 | missense variant | A/C;G | snv | 4.0E-06; 0.48 | 7 | ||
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 | 2 | |||
rs1250552 | 0.882 | 0.200 | 10 | 79298270 | intron variant | A/C;G | snv | 1 | |||
rs13010713 | 0.882 | 0.200 | 2 | 181131318 | intron variant | A/C;G | snv | 1 | |||
rs6848139 | 1.000 | 0.040 | 4 | 122473886 | intergenic variant | A/C;G | snv | 1 | |||
rs9792269 | 0.882 | 0.200 | 8 | 128252343 | intergenic variant | A/C;G | snv | 1 | |||
rs11145763 | 0.724 | 0.240 | 9 | 136369144 | intron variant | A/C;G;T | snv | 14 | |||
rs391851 | 0.882 | 5 | 103342219 | intergenic variant | A/C;G;T | snv | 4 | ||||
rs8061370 | 0.882 | 16 | 11364614 | intron variant | A/C;T | snv | 4 | ||||
rs8192284 | 0.724 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 3 | |||
rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 34 | |
rs4625 | 0.716 | 0.280 | 3 | 49534707 | 3 prime UTR variant | A/G | snv | 0.30 | 17 | ||
rs12598357 | 0.724 | 0.240 | 16 | 28329624 | intergenic variant | A/G | snv | 0.43 | 15 | ||
rs17466626 | 0.724 | 0.240 | 12 | 40366829 | non coding transcript exon variant | A/G | snv | 1.7E-02 | 14 | ||
rs72743477 | 0.724 | 0.240 | 15 | 67171953 | intron variant | A/G | snv | 0.17 | 14 | ||
rs1893217 | 0.742 | 0.440 | 18 | 12809341 | intron variant | A/G | snv | 0.12 | 10 | ||
rs10425559 | 0.807 | 0.040 | 19 | 4837475 | upstream gene variant | A/G | snv | 0.66 | 7 | ||
rs7441808 | 0.851 | 0.040 | 4 | 26088753 | intron variant | A/G | snv | 0.20 | 5 | ||
rs12980063 | 0.882 | 19 | 49693735 | intron variant | A/G | snv | 0.48 | 4 | |||
rs1320344 | 0.882 | 12 | 103493699 | intron variant | A/G | snv | 0.64 | 4 |