Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs1800896 | 0.507 | 0.800 | 1 | 206773552 | intron variant | T/C | snv | 0.41 | 113 | ||
rs2228145 | 0.602 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 0.38; 1.2E-05 | 57 | ||
rs61816761 | 0.658 | 0.640 | 1 | 152313385 | stop gained | G/A;T | snv | 9.4E-03; 8.0E-06 | 43 | ||
rs35829419 | 0.689 | 0.560 | 1 | 247425556 | missense variant | C/A | snv | 3.9E-02 | 3.3E-02 | 23 | |
rs138726443 | 0.790 | 0.200 | 1 | 152307547 | stop gained | G/A;C;T | snv | 2.8E-03; 4.0E-06; 1.6E-05 | 7 | ||
rs11584340 | 0.827 | 0.200 | 1 | 152313454 | missense variant | G/A | snv | 0.27 | 0.19 | 5 | |
rs150597413 | 0.827 | 0.160 | 1 | 152305146 | stop gained | G/A;C;T | snv | 3.6E-05; 4.0E-06; 1.5E-03 | 5 | ||
rs2427837 | 0.851 | 0.160 | 1 | 159288755 | upstream gene variant | G/A | snv | 0.20 | 5 | ||
rs3126085 | 0.851 | 0.280 | 1 | 152328341 | intron variant | G/A | snv | 0.29 | 5 | ||
rs941934 | 0.851 | 0.200 | 1 | 152417976 | intron variant | T/A;C | snv | 5 | |||
rs121909626 | 0.882 | 0.120 | 1 | 152307225 | stop gained | G/C;T | snv | 2.0E-05 | 4 | ||
rs146466242 | 0.851 | 0.120 | 1 | 152302822 | stop gained | T/A;C | snv | 1.4E-03; 8.0E-06 | 4 | ||
rs6684514 | 0.925 | 0.120 | 1 | 156285665 | missense variant | G/A | snv | 0.27 | 0.24 | 4 | |
rs7512552 | 1.000 | 0.120 | 1 | 150293284 | upstream gene variant | T/C | snv | 0.63 | 4 | ||
rs115746363 | 0.882 | 0.120 | 1 | 152312410 | stop gained | G/A;C | snv | 6.0E-04 | 3 | ||
rs149484917 | 0.882 | 0.120 | 1 | 152304939 | stop gained | G/C;T | snv | 4.7E-04; 4.0E-06 | 3 | ||
rs2251746 | 0.882 | 0.120 | 1 | 159302270 | intron variant | T/C | snv | 0.20 | 3 | ||
rs3001978 | 0.882 | 0.160 | 1 | 152153991 | 3 prime UTR variant | T/C | snv | 0.50 | 3 | ||
rs7534334 | 0.882 | 0.160 | 1 | 153205376 | downstream gene variant | C/T | snv | 0.25 | 3 | ||
rs761212672 | 0.882 | 0.120 | 1 | 152304999 | stop gained | G/T | snv | 3.2E-05 | 3 | ||
rs11204971 | 0.925 | 0.120 | 1 | 152286602 | intron variant | A/G | snv | 0.15 | 2 | ||
rs113136594 | 0.925 | 0.120 | 1 | 152313436 | missense variant | G/A;C;T | snv | 6.0E-04; 4.0E-06; 8.0E-06 | 2 | ||
rs12081541 | 0.925 | 0.160 | 1 | 152468890 | intergenic variant | T/C | snv | 8.9E-02 | 2 | ||
rs12130219 | 0.925 | 0.120 | 1 | 152189630 | non coding transcript exon variant | A/G | snv | 0.23 | 2 |