Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2072671 | 0.752 | 0.280 | 1 | 20589208 | missense variant | A/C | snv | 0.28 | 0.25 | 16 | |
rs60369023 | 0.851 | 0.240 | 1 | 20604981 | missense variant | G/A | snv | 2.6E-04 | 1.5E-04 | 4 | |
rs1225118391 | 0.925 | 0.200 | 1 | 230710637 | missense variant | T/C | snv | 4.0E-06 | 2 | ||
rs560299246 | 0.925 | 0.200 | 1 | 241858594 | missense variant | C/T | snv | 8.0E-05 | 7.0E-06 | 2 | |
rs746983719 | 0.925 | 0.200 | 1 | 241860647 | missense variant | T/C | snv | 1.2E-05 | 2 | ||
rs764493111 | 0.925 | 0.200 | 1 | 241858654 | missense variant | G/A;T | snv | 8.0E-06; 8.0E-06 | 2 | ||
rs770085172 | 1.000 | 0.160 | 1 | 230710315 | missense variant | T/C | snv | 7.0E-06 | 1 | ||
rs369137693 | 0.925 | 0.200 | 2 | 69193414 | missense variant | C/T | snv | 2.8E-05 | 1.4E-05 | 2 | |
rs747908253 | 0.925 | 0.200 | 2 | 69182599 | missense variant | G/A | snv | 1.6E-05 | 2 | ||
rs1052133 | 0.476 | 0.800 | 3 | 9757089 | missense variant | C/G | snv | 0.27 | 0.22 | 147 | |
rs746702110 | 0.627 | 0.480 | 3 | 9756778 | missense variant | C/T | snv | 1.2E-05 | 2.8E-05 | 38 | |
rs767551092 | 0.790 | 0.200 | 3 | 14164838 | missense variant | G/A | snv | 4.0E-06 | 10 | ||
rs2227928 | 0.851 | 0.200 | 3 | 142562770 | missense variant | A/G | snv | 0.55 | 0.63 | 6 | |
rs77907221 | 0.882 | 0.160 | 3 | 14154795 | intron variant | AATATTTATAAATATTATAAATTTATTTATATATATAAATATATATAATTTATAAATATTATAAATTATTATAAAAAATT/- | delins | 3 | |||
rs1180868926 | 0.925 | 0.200 | 3 | 9757095 | missense variant | A/G | snv | 4.0E-06 | 2 | ||
rs373917450 | 0.925 | 0.160 | 3 | 14158365 | missense variant | G/T | snv | 4.0E-06 | 2 | ||
rs761032372 | 0.925 | 0.200 | 3 | 9759215 | missense variant | C/A;T | snv | 8.0E-06 | 2 | ||
rs778990691 | 0.807 | 0.240 | 5 | 87395069 | missense variant | A/G | snv | 4.0E-06 | 6 | ||
rs4880 | 0.500 | 0.840 | 6 | 159692840 | missense variant | A/G | snv | 0.48 | 0.47 | 131 | |
rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
rs3218536 | 0.620 | 0.440 | 7 | 152648922 | missense variant | C/G;T | snv | 4.0E-06; 6.4E-02 | 37 | ||
rs2066853 | 0.653 | 0.600 | 7 | 17339486 | missense variant | G/A | snv | 0.15 | 0.22 | 34 | |
rs2227983 | 0.658 | 0.520 | 7 | 55161562 | missense variant | G/A;C;T | snv | 0.29 | 31 | ||
rs1405999227 | 0.925 | 0.160 | 7 | 55156637 | missense variant | A/G | snv | 4.0E-06 | 3 | ||
rs1160237842 | 1.000 | 0.160 | 7 | 151078668 | missense variant | A/G | snv | 8.0E-06 | 2 |