Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11190870 | 0.827 | 0.200 | 10 | 101219450 | intergenic variant | T/A;C | snv | 4 | |||
rs11598177 | 1.000 | 0.040 | 10 | 101220399 | regulatory region variant | T/C | snv | 0.47 | 1 | ||
rs1322332 | 1.000 | 0.040 | 10 | 101222891 | downstream gene variant | T/C | snv | 0.50 | 1 | ||
rs1407409 | 1.000 | 0.040 | 10 | 101225650 | upstream gene variant | T/C | snv | 0.22 | 1 | ||
rs1535462 | 1.000 | 0.040 | 10 | 101214115 | TF binding site variant | A/C;G | snv | 1 | |||
rs200590764 | 1.000 | 0.040 | 10 | 101216904 | intergenic variant | -/T | delins | 6.6E-03 | 1 | ||
rs3950032 | 1.000 | 0.040 | 10 | 101214352 | TF binding site variant | A/C;G;T | snv | 1 | |||
rs76319884 | 1.000 | 0.040 | 10 | 101216249 | intergenic variant | C/G | snv | 8.8E-02 | 1 | ||
rs7914775 | 1.000 | 0.040 | 10 | 101216904 | intergenic variant | C/T | snv | 8.8E-02 | 1 | ||
rs1557055405 | 0.807 | 0.400 | X | 153743532 | missense variant | T/A | snv | 21 | |||
rs6570507 | 0.827 | 0.240 | 6 | 142358435 | intron variant | G/A | snv | 0.47 | 11 | ||
rs864321670 | 0.763 | 0.320 | 10 | 95633012 | missense variant | C/T | snv | 24 | |||
rs369160589 | 0.742 | 0.400 | 16 | 5082676 | splice region variant | A/G | snv | 1.0E-04 | 1.3E-04 | 35 | |
rs1009298200 | 0.742 | 0.400 | 16 | 5079077 | missense variant | C/G;T | snv | 7.0E-06 | 34 | ||
rs1555452127 | 0.742 | 0.400 | 16 | 5079078 | missense variant | T/C | snv | 34 | |||
rs1553403917 | 0.807 | 0.320 | 2 | 73451171 | frameshift variant | -/A | delins | 7 | |||
rs1569324457 | 0.851 | 0.280 | 20 | 32433481 | frameshift variant | AG/- | del | 7 | |||
rs797045412 | 0.776 | 0.280 | 9 | 92718565 | missense variant | G/A;T | snv | 17 | |||
rs1555968941 | 0.752 | 0.280 | 12 | 2653847 | missense variant | G/A;C | snv | 31 | |||
rs1057518891 | 0.851 | 0.120 | 8 | 60854479 | stop gained | C/T | snv | 6 | |||
rs10510181 | 0.882 | 0.200 | 3 | 149364 | intron variant | G/A | snv | 0.31 | 3 | ||
rs1568097 | 1.000 | 0.040 | 3 | 138468 | intron variant | T/C | snv | 0.42 | 1 | ||
rs1588962 | 1.000 | 0.040 | 3 | 142352 | intron variant | T/C | snv | 0.32 | 1 | ||
rs4684051 | 1.000 | 0.040 | 3 | 136842 | intron variant | A/G | snv | 0.34 | 1 | ||
rs1400180 | 1.000 | 0.040 | 3 | 129285 | intron variant | T/G | snv | 0.37 | 1 |