Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1260333 | 0.882 | 0.160 | 2 | 27525757 | downstream gene variant | A/G | snv | 0.58 | 12 | ||
rs579383 | 11 | 61769111 | intron variant | G/A | snv | 0.58 | 2 | ||||
rs174574 | 1.000 | 0.080 | 11 | 61832870 | intron variant | A/C | snv | 0.55 | 7 | ||
rs4713103 | 6 | 10968908 | intron variant | G/T | snv | 0.55 | 1 | ||||
rs2295602 | 6 | 11005609 | intron variant | T/C | snv | 0.57 | 0.54 | 1 | |||
rs174449 | 11 | 61872907 | downstream gene variant | G/A | snv | 0.54 | 2 | ||||
rs1570069 | 6 | 11017592 | intron variant | A/G | snv | 0.54 | 1 | ||||
rs7743830 | 6 | 11013987 | intron variant | A/G | snv | 0.54 | 1 | ||||
rs13966 | 11 | 61897520 | 3 prime UTR variant | T/C | snv | 0.53 | 1 | ||||
rs6900220 | 6 | 11064905 | intron variant | T/C | snv | 0.53 | 1 | ||||
rs2147041 | 6 | 11050290 | intron variant | A/G | snv | 0.53 | 1 | ||||
rs3798707 | 6 | 10991702 | intron variant | C/T | snv | 0.53 | 1 | ||||
rs12587311 | 14 | 28647489 | intergenic variant | T/C | snv | 0.53 | 1 | ||||
rs3845427 | 1 | 181293302 | intergenic variant | T/A | snv | 0.52 | 1 | ||||
rs509360 | 11 | 61781087 | intron variant | A/G | snv | 0.61 | 0.52 | 3 | |||
rs3798711 | 6 | 11002577 | intron variant | T/C | snv | 0.52 | 1 | ||||
rs1424760 | 2 | 162925277 | intergenic variant | C/T | snv | 0.52 | 1 | ||||
rs174616 | 1.000 | 0.080 | 11 | 61861650 | intron variant | G/A | snv | 0.51 | 3 | ||
rs8012543 | 14 | 28618344 | upstream gene variant | G/A | snv | 0.50 | 1 | ||||
rs7773173 | 6 | 10956470 | intron variant | G/C | snv | 0.50 | 1 | ||||
rs2391388 | 1 | 95020269 | intron variant | A/C | snv | 0.49 | 2 | ||||
rs174626 | 11 | 61869585 | downstream gene variant | G/A | snv | 0.48 | 2 | ||||
rs102275 | 0.827 | 0.320 | 11 | 61790331 | non coding transcript exon variant | T/C | snv | 0.47 | 18 | ||
rs198476 | 11 | 61758258 | intron variant | G/A | snv | 0.46 | 1 | ||||
rs198462 | 11 | 61756647 | intron variant | G/A | snv | 0.46 | 1 |