Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7574865 | 0.574 | 0.720 | 2 | 191099907 | intron variant | T/G | snv | 0.79 | 59 | ||
rs1520220 | 0.807 | 0.280 | 12 | 102402744 | intron variant | G/C;T | snv | 0.76 | 9 | ||
rs1861494 | 0.716 | 0.400 | 12 | 68157629 | intron variant | C/T | snv | 0.75 | 15 | ||
rs2910164 | 0.447 | 0.880 | 5 | 160485411 | mature miRNA variant | C/G | snv | 0.71; 4.1E-06 | 0.70 | 193 | |
rs4288398 | 1.000 | 0.120 | 8 | 7024116 | downstream gene variant | A/G | snv | 0.70 | 1 | ||
rs4646 | 0.716 | 0.360 | 15 | 51210647 | 3 prime UTR variant | A/C | snv | 0.67 | 0.70 | 16 | |
rs7763262 | 1.000 | 0.120 | 6 | 32457105 | downstream gene variant | T/C | snv | 0.70 | 1 | ||
rs2070744 | 0.608 | 0.680 | 7 | 150992991 | intron variant | C/T | snv | 0.70 | 54 | ||
rs1800871 | 0.508 | 0.800 | 1 | 206773289 | 5 prime UTR variant | A/G | snv | 0.69 | 108 | ||
rs1800872 | 0.495 | 0.840 | 1 | 206773062 | 5 prime UTR variant | T/G | snv | 0.69 | 119 | ||
rs4227 | 1.000 | 0.120 | 17 | 7587859 | 3 prime UTR variant | G/T | snv | 0.71 | 0.67 | 2 | |
rs9275596 | 0.827 | 0.280 | 6 | 32713854 | upstream gene variant | C/T | snv | 0.66 | 7 | ||
rs2856717 | 1.000 | 0.120 | 6 | 32702531 | downstream gene variant | A/G | snv | 0.64 | 2 | ||
rs12022418 | 1.000 | 0.120 | 1 | 192565977 | intron variant | C/A | snv | 0.64 | 1 | ||
rs3803800 | 0.807 | 0.240 | 17 | 7559652 | missense variant | A/G | snv | 0.70 | 0.64 | 7 | |
rs11264794 | 1.000 | 0.120 | 1 | 157677999 | 3 prime UTR variant | C/A | snv | 0.63 | 2 | ||
rs9314614 | 1.000 | 0.120 | 8 | 6840209 | intron variant | C/G | snv | 0.61 | 2 | ||
rs1055901 | 1.000 | 0.120 | 18 | 63805221 | 3 prime UTR variant | T/C | snv | 0.61 | 1 | ||
rs1946518 | 0.602 | 0.760 | 11 | 112164735 | intron variant | T/G | snv | 0.60 | 46 | ||
rs1055902 | 1.000 | 0.120 | 18 | 63805309 | 3 prime UTR variant | C/T | snv | 0.59 | 1 | ||
rs699 | 0.501 | 0.800 | 1 | 230710048 | missense variant | A/G | snv | 0.55 | 0.58 | 134 | |
rs16944 | 0.531 | 0.920 | 2 | 112837290 | upstream gene variant | A/G | snv | 0.57 | 92 | ||
rs2738058 | 0.925 | 0.160 | 8 | 6964095 | upstream gene variant | T/C | snv | 0.57 | 2 | ||
rs2412971 | 0.882 | 0.320 | 22 | 30098382 | intron variant | G/A | snv | 0.55 | 5 | ||
rs11102930 | 0.925 | 0.160 | 1 | 115338434 | intron variant | G/A | snv | 0.54 | 2 |