Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7692976 | 1.000 | 0.040 | 4 | 109990411 | intron variant | A/G;T | snv | 2 | |||
rs10905928 | 1.000 | 0.040 | 10 | 11300924 | intron variant | C/A | snv | 0.21 | 1 | ||
rs1190286 | 1.000 | 0.040 | 6 | 105163071 | intron variant | C/T | snv | 0.66 | 1 | ||
rs13402990 | 1.000 | 0.040 | 2 | 70231632 | intron variant | A/T | snv | 9.7E-03 | 1 | ||
rs151139112 | 1.000 | 0.040 | 12 | 120322275 | missense variant | C/T | snv | 8.9E-04 | 3.2E-03 | 1 | |
rs2277212 | 1.000 | 0.040 | 10 | 11257772 | synonymous variant | A/T | snv | 0.75 | 0.74 | 1 | |
rs2298991 | 1.000 | 0.040 | 4 | 109970856 | intron variant | T/A;G | snv | 1 | |||
rs2515475 | 1.000 | 0.040 | 8 | 6530918 | intron variant | C/T | snv | 0.19 | 1 | ||
rs2592178 | 1.000 | 0.040 | 2 | 70245350 | intron variant | G/A | snv | 0.27 | 1 | ||
rs34568801 | 1.000 | 0.040 | 1 | 19975708 | missense variant | C/T | snv | 4.6E-03 | 4.3E-03 | 1 | |
rs3814634 | 1.000 | 0.040 | 10 | 11099442 | splice region variant | G/T | snv | 0.37 | 1 | ||
rs3848719 | 1.000 | 0.040 | 20 | 45967906 | synonymous variant | G/A | snv | 0.33 | 0.32 | 1 | |
rs4698803 | 1.000 | 0.040 | 4 | 109993271 | missense variant | A/G;T | snv | 0.85 | 1 | ||
rs516651 | 1.000 | 0.040 | 1 | 231406910 | intron variant | C/T | snv | 0.15 | 1 | ||
rs6533485 | 1.000 | 0.040 | 4 | 110006407 | intron variant | G/C | snv | 0.61 | 1 | ||
rs672961 | 1.000 | 0.040 | 1 | 70101505 | intron variant | C/G | snv | 0.99 | 1 | ||
rs7068124 | 1.000 | 0.040 | 10 | 11023453 | intron variant | T/C;G | snv | 1 | |||
rs78142040 | 1.000 | 0.040 | X | 2914730 | non coding transcript exon variant | C/T | snv | 1 | |||
rs782230926 | 1.000 | 0.040 | 17 | 41734538 | missense variant | G/T | snv | 8.4E-06 | 7.0E-06 | 1 | |
rs9605146 | 1.000 | 0.040 | 22 | 16784304 | missense variant | G/A | snv | 0.39 | 1 | ||
rs117603931 | 0.882 | 0.080 | 16 | 2319591 | missense variant | C/T | snv | 5.7E-03 | 6.5E-03 | 4 | |
rs121434431 | 0.851 | 0.080 | 4 | 186083346 | missense variant | C/T | snv | 4.1E-04 | 5.2E-04 | 4 | |
rs3774934 | 0.851 | 0.080 | 4 | 102506319 | intron variant | A/C;G;T | snv | 4 | |||
rs146709251 | 0.882 | 0.080 | 16 | 2279070 | missense variant | G/A | snv | 4.3E-03 | 3.0E-03 | 3 | |
rs761495176 | 0.882 | 0.080 | 5 | 143400263 | missense variant | T/C | snv | 1.7E-05 | 3 |