Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1206846668 | 0.724 | 0.400 | 11 | 49185773 | missense variant | G/A | snv | 4.1E-06 | 16 | ||
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs121913459 | 0.672 | 0.160 | 9 | 130872896 | missense variant | C/T | snv | 25 | |||
rs12402181 | 0.882 | 0.120 | 1 | 66628488 | mature miRNA variant | G/A | snv | 0.17 | 0.24 | 3 | |
rs12434881 | 0.882 | 0.120 | 14 | 23119433 | 5 prime UTR variant | G/A | snv | 0.36 | 3 | ||
rs1275561861 | 0.672 | 0.360 | 6 | 29944350 | missense variant | G/A | snv | 23 | |||
rs12803915 | 0.882 | 0.120 | 11 | 65444508 | non coding transcript exon variant | G/A | snv | 0.16 | 0.17 | 3 | |
rs1296957097 | 0.882 | 0.120 | 22 | 28719401 | missense variant | A/G | snv | 3 | |||
rs1310678797 | 0.882 | 0.120 | 12 | 47857143 | missense variant | C/T | snv | 7.0E-06 | 3 | ||
rs1361742125 | 0.882 | 0.120 | 5 | 143399842 | missense variant | T/C | snv | 4.0E-06 | 7.0E-06 | 3 | |
rs138047632 | 0.882 | 0.120 | 21 | 45525860 | missense variant | A/G | snv | 2.4E-03 | 2.2E-03 | 3 | |
rs140422742 | 0.882 | 0.120 | 7 | 99778046 | missense variant | T/C;G | snv | 7.6E-05 | 6.3E-05 | 3 | |
rs1412792500 | 0.882 | 0.120 | 5 | 143400541 | missense variant | T/C | snv | 4.0E-06 | 1.4E-05 | 3 | |
rs1427331568 | 0.882 | 0.120 | 5 | 143314010 | missense variant | G/C | snv | 3 | |||
rs143125661 | 0.882 | 0.120 | 6 | 18149120 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 3 | |
rs1448674651 | 0.667 | 0.560 | 18 | 671384 | missense variant | G/A;C | snv | 4.0E-06 | 23 | ||
rs1470755915 | 0.776 | 0.240 | 8 | 92005229 | missense variant | C/A | snv | 7.0E-06 | 10 | ||
rs1482545954 | 0.882 | 0.120 | 19 | 54982407 | missense variant | C/T | snv | 7.0E-06 | 3 | ||
rs153109 | 0.623 | 0.600 | 16 | 28507775 | intron variant | T/C | snv | 0.43 | 37 | ||
rs1544105 | 0.851 | 0.200 | 9 | 127800446 | intron variant | C/T | snv | 0.48 | 4 | ||
rs1573613 | 0.882 | 0.120 | 12 | 11894684 | 3 prime UTR variant | T/C | snv | 0.48 | 3 | ||
rs16754 | 0.732 | 0.240 | 11 | 32396399 | synonymous variant | T/C | snv | 0.24; 4.0E-06 | 0.17 | 15 | |
rs1695 | 0.457 | 0.880 | 11 | 67585218 | missense variant | A/G | snv | 0.34 | 0.36 | 188 | |
rs17007695 | 0.851 | 0.120 | 4 | 141788570 | intergenic variant | T/C | snv | 7.7E-02 | 4 | ||
rs17069665 | 0.882 | 0.120 | 6 | 108620265 | intron variant | A/C;G | snv | 4 |