Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4759314 | 0.649 | 0.440 | 12 | 53968051 | non coding transcript exon variant | G/A | snv | 0.93 | 31 | ||
rs4635002 | 0.925 | 0.080 | 10 | 127064415 | intron variant | A/C | snv | 0.92 | 3 | ||
rs1760893 | 0.807 | 0.080 | 14 | 20412501 | intron variant | C/A | snv | 0.89 | 6 | ||
rs629367 | 0.776 | 0.200 | 11 | 122146306 | intron variant | C/A | snv | 0.88 | 11 | ||
rs7853122 | 0.925 | 0.080 | 9 | 131705224 | intron variant | C/T | snv | 0.87 | 3 | ||
rs40239 | 0.851 | 0.120 | 7 | 116677823 | intron variant | G/A | snv | 0.87 | 4 | ||
rs1279599 | 0.925 | 0.080 | 6 | 110879025 | intron variant | G/A | snv | 0.87 | 2 | ||
rs2494752 | 0.790 | 0.120 | 14 | 104797271 | upstream gene variant | A/G | snv | 0.85 | 10 | ||
rs1047972 | 0.716 | 0.240 | 20 | 56386407 | missense variant | T/C | snv | 0.85 | 0.84 | 19 | |
rs1051690 | 0.851 | 0.080 | 19 | 7116952 | 3 prime UTR variant | T/C | snv | 0.83 | 4 | ||
rs1679709 | 0.925 | 0.080 | 6 | 28260564 | missense variant | A/G | snv | 0.87 | 0.83 | 2 | |
rs5030625 | 0.882 | 0.160 | 16 | 68736944 | upstream gene variant | A/- | del | 0.80 | 3 | ||
rs1864169 | 0.851 | 0.200 | 14 | 81203689 | intron variant | G/T | snv | 0.78 | 5 | ||
rs526934 | 0.925 | 0.080 | 11 | 59866020 | intron variant | G/A | snv | 0.77 | 2 | ||
rs751402 | 0.724 | 0.360 | 13 | 102845848 | 5 prime UTR variant | A/G | snv | 0.76 | 15 | ||
rs1520220 | 0.807 | 0.280 | 12 | 102402744 | intron variant | G/C;T | snv | 0.76 | 9 | ||
rs8193036 | 0.689 | 0.600 | 6 | 52185695 | upstream gene variant | C/T | snv | 0.72 | 21 | ||
rs25487 | 0.441 | 0.800 | 19 | 43551574 | missense variant | T/C | snv | 0.68 | 0.71 | 205 | |
rs1800795 | 0.494 | 0.840 | 7 | 22727026 | intron variant | C/G | snv | 0.71 | 140 | ||
rs2910164 | 0.447 | 0.880 | 5 | 160485411 | mature miRNA variant | C/G | snv | 0.71; 4.1E-06 | 0.70 | 193 | |
rs10022537 | 0.925 | 0.080 | 4 | 16075214 | intron variant | A/T | snv | 0.70 | 2 | ||
rs461404 | 0.925 | 0.080 | 5 | 40799438 | upstream gene variant | G/A | snv | 0.70 | 3 | ||
rs1635566 | 1.000 | 0.080 | 1 | 17356662 | intron variant | A/G | snv | 0.70 | 1 | ||
rs2070744 | 0.608 | 0.680 | 7 | 150992991 | intron variant | C/T | snv | 0.70 | 53 | ||
rs10421916 | 0.925 | 0.080 | 19 | 17818178 | intron variant | A/G | snv | 0.69 | 2 |