Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs28934897 | 0.790 | 0.400 | 12 | 109596515 | missense variant | G/A | snv | 1.6E-03 | 1.5E-03 | 10 | |
rs104895304 | 0.827 | 0.280 | 12 | 109591275 | missense variant | T/C | snv | 1.5E-04 | 1.7E-04 | 5 | |
rs104895301 | 0.851 | 0.240 | 12 | 109586098 | missense variant | G/A | snv | 4.0E-06 | 1.4E-05 | 4 | |
rs104895317 | 0.851 | 0.280 | 12 | 109595142 | missense variant | G/A | snv | 9.6E-05 | 6.3E-05 | 4 | |
rs104895319 | 0.851 | 0.240 | 12 | 109595070 | missense variant | G/A | snv | 2.0E-05 | 7.0E-06 | 4 | |
rs104895321 | 0.882 | 0.240 | 12 | 109591301 | missense variant | C/G;T | snv | 1.4E-04 | 4 | ||
rs104895382 | 0.851 | 0.240 | 12 | 109579921 | missense variant | T/C | snv | 3.2E-05 | 7.0E-05 | 4 | |
rs4149637 | 0.851 | 0.320 | 12 | 6333835 | missense variant | G/A;C | snv | 5.7E-03 | 4 | ||
rs104895322 | 0.882 | 0.240 | 12 | 109574893 | frameshift variant | -/T | delins | 3 | |||
rs104895297 | 0.882 | 0.360 | 12 | 109581427 | missense variant | C/T | snv | 3 | |||
rs104895308 | 0.882 | 0.200 | 12 | 109595118 | missense variant | G/A | snv | 3 | |||
rs104895324 | 0.882 | 0.240 | 12 | 109596525 | missense variant | A/G | snv | 3.6E-05 | 4.9E-05 | 3 | |
rs104895332 | 0.882 | 0.240 | 12 | 109586102 | missense variant | T/C | snv | 1.2E-05 | 3.5E-05 | 3 | |
rs104895352 | 0.882 | 0.240 | 12 | 109591302 | missense variant | G/A | snv | 8.0E-06 | 2.1E-05 | 3 | |
rs1566147222 | 0.882 | 0.240 | 12 | 109586039 | stop gained | T/A | snv | 3 | |||
rs104895295 | 0.925 | 0.200 | 12 | 109574881 | missense variant | A/C;G | snv | 4.1E-06; 4.1E-06 | 2 | ||
rs104895316 | 0.925 | 0.200 | 12 | 109591266 | missense variant | T/C;G | snv | 2 | |||
rs104895335 | 1.000 | 0.200 | 12 | 109574882 | missense variant | T/A;C | snv | 8.2E-06 | 1 | ||
rs11544299 | 1.000 | 0.200 | 12 | 109574880 | missense variant | C/A;T | snv | 1 | |||
rs104895296 | 1.000 | 0.200 | 12 | 109576035 | missense variant | T/C | snv | 1 | |||
rs104895298 | 1.000 | 0.200 | 12 | 109581465 | missense variant | G/A | snv | 3.5E-05 | 1 | ||
rs104895300 | 1.000 | 0.200 | 12 | 109581523 | missense variant | C/T | snv | 8.0E-06 | 1 | ||
rs104895303 | 1.000 | 0.200 | 12 | 109586766 | missense variant | G/A;T | snv | 2.0E-05 | 1 | ||
rs104895305 | 1.000 | 0.200 | 12 | 109595067 | missense variant | G/A;C | snv | 8.0E-06; 4.0E-06 | 1 | ||
rs104895323 | 1.000 | 0.200 | 12 | 109581441 | frameshift variant | G/-;GG | delins | 1 |