Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1461729 | 1.000 | 8 | 9329732 | intron variant | A/G | snv | 0.88 | 5 | |||
rs6601299 | 0.925 | 0.040 | 8 | 9327181 | intron variant | T/C | snv | 0.88 | 5 | ||
rs2126259 | 1.000 | 8 | 9327636 | intron variant | T/C | snv | 0.87 | 9 | |||
rs12447924 | 1.000 | 16 | 56960280 | upstream gene variant | C/T | snv | 0.76 | 3 | |||
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 81 | |
rs780094 | 0.658 | 0.400 | 2 | 27518370 | intron variant | T/C | snv | 0.67 | 62 | ||
rs10741657 | 0.637 | 0.520 | 11 | 14893332 | upstream gene variant | A/G | snv | 0.65 | 34 | ||
rs7946 | 0.851 | 0.160 | 17 | 17506246 | missense variant | C/T | snv | 0.59 | 0.59 | 6 | |
rs3480 | 0.807 | 0.160 | 1 | 32862564 | 3 prime UTR variant | G/A | snv | 0.56 | 8 | ||
rs2645424 | 0.827 | 0.120 | 8 | 11826954 | intron variant | A/C;G | snv | 0.56 | 5 | ||
rs4674344 | 1.000 | 2 | 218805152 | intron variant | A/T | snv | 0.53 | 1 | |||
rs6006469 | 1.000 | 22 | 43987737 | non coding transcript exon variant | C/G | snv | 0.49 | 1 | |||
rs12743824 | 0.925 | 0.040 | 1 | 99317401 | intergenic variant | C/A | snv | 0.48 | 2 | ||
rs2235778 | 1.000 | 22 | 43993634 | intron variant | T/C | snv | 0.48 | 1 | |||
rs3788604 | 1.000 | 22 | 43992537 | intron variant | A/G | snv | 0.48 | 1 | |||
rs6006468 | 1.000 | 22 | 43987552 | non coding transcript exon variant | G/C | snv | 0.48 | 1 | |||
rs6006602 | 1.000 | 22 | 43987520 | non coding transcript exon variant | C/T | snv | 0.48 | 1 | |||
rs4880 | 0.500 | 0.840 | 6 | 159692840 | missense variant | A/G | snv | 0.48 | 0.47 | 131 | |
rs2281292 | 1.000 | 22 | 43999509 | intron variant | A/C | snv | 0.44 | 0.47 | 1 | ||
rs6006473 | 0.925 | 0.040 | 22 | 43997195 | intron variant | C/T | snv | 0.47 | 2 | ||
rs4823182 | 0.925 | 0.080 | 22 | 43981562 | intron variant | A/G | snv | 0.46 | 2 | ||
rs9940128 | 0.851 | 0.120 | 16 | 53766842 | intron variant | G/A | snv | 0.42 | 10 | ||
rs9939609 | 0.559 | 0.720 | 16 | 53786615 | intron variant | T/A | snv | 0.41 | 98 | ||
rs8050136 | 0.716 | 0.560 | 16 | 53782363 | intron variant | C/A | snv | 0.40 | 32 | ||
rs2071303 | 0.882 | 0.120 | 6 | 26091108 | splice region variant | T/C | snv | 0.38 | 0.36 | 6 |