Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4647924 | 0.600 | 0.520 | 4 | 1801844 | missense variant | C/A;G;T | snv | 4.2E-06; 4.2E-06 | 49 | ||
rs121913482 | 0.630 | 0.680 | 4 | 1801837 | missense variant | C/T | snv | 45 | |||
rs121913483 | 0.649 | 0.560 | 4 | 1801841 | missense variant | C/A;G;T | snv | 4.2E-06; 1.3E-05 | 31 | ||
rs121913105 | 0.653 | 0.600 | 4 | 1806163 | missense variant | A/C;T | snv | 30 | |||
rs28933068 | 0.645 | 0.560 | 4 | 1805644 | missense variant | C/A;G;T | snv | 1.6E-05 | 30 | ||
rs78311289 | 0.689 | 0.440 | 4 | 1806162 | missense variant | A/C;G | snv | 4.0E-06 | 25 | ||
rs28931614 | 0.672 | 0.520 | 4 | 1804392 | missense variant | G/A;C | snv | 21 | |||
rs121913485 | 0.716 | 0.400 | 4 | 1804372 | missense variant | A/G | snv | 18 | |||
rs28931615 | 0.732 | 0.240 | 4 | 1804426 | missense variant | C/A;T | snv | 13 | |||
rs121913479 | 0.763 | 0.280 | 4 | 1804362 | missense variant | G/A;T | snv | 4.0E-06 | 10 | ||
rs121913116 | 0.763 | 0.360 | 4 | 1799395 | missense variant | C/T | snv | 9 | |||
rs1211533350 | 0.827 | 0.120 | 4 | 1805638 | synonymous variant | C/A | snv | 4.0E-06 | 7.0E-06 | 5 | |
rs121913484 | 0.851 | 0.240 | 4 | 1804365 | missense variant | A/T | snv | 5 | |||
rs587779383 | 0.851 | 0.120 | 4 | 1806157 | missense variant | A/C;G;T | snv | 5 | |||
rs886043613 | 0.925 | 0.080 | 4 | 1801519 | missense variant | C/T | snv | 4 | |||
rs121913101 | 0.882 | 0.080 | 4 | 1807260 | stop lost | T/A;C;G | snv | 3 | |||
rs121913113 | 0.882 | 0.240 | 4 | 1806076 | missense variant | G/A | snv | 3 | |||
rs17881656 | 0.925 | 0.240 | 4 | 1804404 | missense variant | T/A;C | snv | 8.0E-06; 3.3E-03 | 3 | ||
rs267606808 | 0.882 | 0.120 | 4 | 1805396 | missense variant | A/G | snv | 3 | |||
rs121913103 | 0.925 | 0.080 | 4 | 1807262 | stop gained | A/C;G;T | snv | 2 | |||
rs121913114 | 0.925 | 0.120 | 4 | 1801930 | missense variant | A/G;T | snv | 4.0E-06 | 2 | ||
rs121913115 | 1.000 | 0.120 | 4 | 1801928 | missense variant | A/G | snv | 2 | |||
rs121913480 | 1.000 | 0.120 | 4 | 1806604 | missense variant | G/T | snv | 2 | |||
rs1325547001 | 1.000 | 0.040 | 4 | 1806619 | missense variant | G/A | snv | 4.0E-06 | 2 | ||
rs1457537911 | 1.000 | 0.160 | 4 | 1801883 | missense variant | A/G | snv | 7.0E-06 | 2 |