Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs35385902 | 0.807 | 0.240 | 4 | 99347122 | missense variant | C/A;T | snv | 2.0E-05; 1.1E-03 | 9 | ||
rs1208 | 0.807 | 0.080 | 8 | 18400806 | missense variant | G/A;T | snv | 0.62; 4.0E-06 | 8 | ||
rs4946936 | 0.790 | 0.160 | 6 | 108682118 | 3 prime UTR variant | T/A;C | snv | 8 | |||
rs749710704 | 0.790 | 0.160 | 5 | 79119289 | missense variant | C/G;T | snv | 4.0E-06; 4.0E-06 | 7 | ||
rs1058172 | 0.882 | 0.080 | 22 | 42127526 | missense variant | C/G;T | snv | 4.4E-06; 9.2E-02 | 4 | ||
rs1629816 | 0.851 | 0.080 | 3 | 10294607 | non coding transcript exon variant | G/A;C | snv | 4 | |||
rs35431622 | 0.851 | 0.120 | 1 | 204190794 | missense variant | T/A;C | snv | 5.5E-05; 4.7E-02 | 4 | ||
rs4855883 | 0.851 | 0.080 | 3 | 49673881 | upstream gene variant | G/A;C | snv | 4 | |||
rs6796803 | 0.925 | 0.040 | 3 | 186746318 | intron variant | T/A;C | snv | 4 | |||
rs762384959 | 0.925 | 0.040 | 14 | 20456680 | missense variant | G/C | snv | 8.0E-06 | 4 | ||
rs763015080 | 0.851 | 0.120 | 4 | 147539821 | missense variant | G/A | snv | 4.1E-06 | 4 | ||
rs985325188 | 0.851 | 0.080 | 14 | 20456806 | missense variant | A/C | snv | 4 | |||
rs1667255 | 0.925 | 0.040 | 18 | 31607316 | intergenic variant | A/C;G;T | snv | 3 | |||
rs752153816 | 0.882 | 0.120 | 6 | 43780848 | missense variant | G/A;C | snv | 4.0E-06; 4.0E-06; 1.2E-05; 3.6E-05 | 3 | ||
rs876659477 | 0.882 | 0.040 | 17 | 7673730 | missense variant | T/C | snv | 3 | |||
rs1183646267 | 0.925 | 0.040 | 11 | 108281026 | missense variant | A/G | snv | 2 | |||
rs16943176 | 0.925 | 0.040 | 17 | 58692526 | upstream gene variant | G/A;C | snv | 2 | |||
rs4253132 | 0.925 | 0.040 | 10 | 49493110 | splice region variant | G/A;T | snv | 0.89; 4.4E-05 | 2 | ||
rs554194414 | 0.925 | 0.040 | 2 | 8731250 | missense variant | T/C | snv | 2 | |||
rs770925903 | 0.925 | 0.040 | 2 | 8731740 | missense variant | C/A;T | snv | 1.6E-05; 4.0E-06 | 2 | ||
rs7802034 | 0.925 | 0.040 | 7 | 152655183 | intron variant | A/C;G | snv | 2 | |||
rs758272654 | 0.611 | 0.680 | 20 | 58909201 | synonymous variant | T/C | snv | 4.0E-06 | 7.0E-06 | 50 | |
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs1297812518 | 0.763 | 0.160 | 14 | 103707168 | missense variant | G/A | snv | 1.3E-05 | 1.4E-05 | 9 | |
rs34612342 | 0.653 | 0.400 | 1 | 45332803 | missense variant | T/C | snv | 1.5E-03 | 1.6E-03 | 32 |