Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10246939 | 0.851 | 0.240 | 7 | 141972804 | missense variant | T/C | snv | 0.49 | 0.47 | 6 | |
rs4880 | 0.500 | 0.840 | 6 | 159692840 | missense variant | A/G | snv | 0.48 | 0.47 | 131 | |
rs2307111 | 0.925 | 0.120 | 5 | 75707853 | missense variant | T/A;C | snv | 4.5E-06; 0.47 | 5 | ||
rs1801394 | 0.531 | 0.840 | 5 | 7870860 | missense variant | A/G | snv | 0.47 | 0.45 | 101 | |
rs4680 | 0.442 | 0.920 | 22 | 19963748 | missense variant | G/A | snv | 0.46 | 0.44 | 249 | |
rs1805096 | 0.827 | 0.200 | 1 | 65636574 | synonymous variant | G/A | snv | 0.46 | 0.43 | 6 | |
rs17848939 | 1.000 | 0.080 | 17 | 82085473 | intron variant | C/G;T | snv | 5.0E-06; 0.45 | 1 | ||
rs2236225 | 0.614 | 0.640 | 14 | 64442127 | missense variant | G/A | snv | 0.44 | 0.38 | 52 | |
rs5498 | 0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 | 99 | |
rs5574 | 0.882 | 0.200 | 7 | 24289514 | synonymous variant | C/T | snv | 0.43 | 0.43 | 5 | |
rs1042713 | 0.576 | 0.800 | 5 | 148826877 | missense variant | G/A | snv | 0.42 | 0.43 | 63 | |
rs12218 | 0.763 | 0.280 | 11 | 18269774 | synonymous variant | T/C | snv | 0.42 | 0.36 | 11 | |
rs660339 | 0.695 | 0.320 | 11 | 73978059 | missense variant | G/A | snv | 0.41 | 0.43 | 24 | |
rs3748024 | 0.925 | 0.080 | 2 | 112588836 | 3 prime UTR variant | C/G | snv | 0.41 | 0.35 | 3 | |
rs4215 | 1.000 | 0.080 | 7 | 99971771 | missense variant | G/A;C | snv | 0.41 | 1 | ||
rs225014 | 0.695 | 0.400 | 14 | 80203237 | missense variant | T/C | snv | 0.41 | 0.39 | 22 | |
rs1799722 | 0.882 | 0.240 | 14 | 96204802 | 5 prime UTR variant | C/T | snv | 0.41 | 0.39 | 4 | |
rs20455 | 0.763 | 0.160 | 6 | 39357302 | missense variant | A/G | snv | 0.41 | 0.49 | 12 | |
rs2229765 | 0.807 | 0.280 | 15 | 98934996 | synonymous variant | G/A | snv | 0.40 | 0.39 | 7 | |
rs12199580 | 1.000 | 0.080 | 6 | 36302353 | missense variant | C/A;T | snv | 0.40 | 1 | ||
rs2228145 | 0.602 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 0.38; 1.2E-05 | 57 | ||
rs662 | 0.485 | 0.840 | 7 | 95308134 | missense variant | T/C | snv | 0.38 | 0.42 | 157 | |
rs11545881 | 0.925 | 0.080 | 18 | 12274105 | missense variant | G/A;C;T | snv | 1.2E-05; 0.37 | 2 | ||
rs180743 | 1.000 | 0.080 | 16 | 28496323 | missense variant | C/G | snv | 0.36 | 0.40 | 1 | |
rs5443 | 0.532 | 0.760 | 12 | 6845711 | synonymous variant | C/T | snv | 0.36 | 0.44 | 106 |