Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs764929617 | 0.776 | 0.200 | 19 | 44907799 | missense variant | C/T | snv | 4.0E-06 | 8 | ||
rs121918398 | 19 | 44909171 | missense variant | G/A | snv | 4.5E-06 | 1 | ||||
rs1466963971 | 0.925 | 0.120 | 19 | 44908640 | missense variant | T/G | snv | 4.5E-06 | 2 | ||
rs11542037 | 1.000 | 0.080 | 19 | 44908657 | missense variant | C/A;T | snv | 5.2E-06 | 1 | ||
rs1458301734 | 1.000 | 0.080 | 19 | 44908687 | missense variant | G/A;T | snv | 5.9E-06 | 1 | ||
rs573658040 | 0.790 | 0.200 | 19 | 44908705 | missense variant | C/G;T | snv | 6.3E-06 | 9 | ||
rs779569800 | 1.000 | 0.080 | 19 | 44908714 | missense variant | G/A;C;T | snv | 1.3E-05; 6.3E-06; 6.3E-06 | 1 | ||
rs387906567 | 0.882 | 0.200 | 19 | 44908774 | missense variant | C/G;T | snv | 6.3E-06 | 4 | ||
rs748703149 | 0.882 | 0.080 | 19 | 44908729 | missense variant | G/A;C;T | snv | 6.3E-06; 6.3E-06 | 3 | ||
rs267606664 | 0.851 | 0.120 | 19 | 44908730 | missense variant | G/A;C | snv | 1.6E-04; 6.3E-06 | 5 | ||
rs121918397 | 0.882 | 0.200 | 19 | 44908784 | missense variant | G/A;C | snv | 6.5E-06 | 3 | ||
rs121918394 | 0.882 | 0.080 | 19 | 44908786 | missense variant | A/C;G | snv | 6.5E-06 | 5 | ||
rs121918395 | 19 | 44909032 | missense variant | C/A;T | snv | 6.9E-06; 4.2E-05 | 1 | ||||
rs267606663 | 0.925 | 0.080 | 19 | 44909021 | missense variant | G/A;C | snv | 7.3E-06 | 3 | ||
rs121918399 | 0.925 | 0.120 | 19 | 44907843 | missense variant | C/T | snv | 8.0E-06 | 2 | ||
rs142480126 | 19 | 44907825 | missense variant | G/A | snv | 8.0E-06 | 1 | ||||
rs533904656 | 1.000 | 0.080 | 19 | 44907768 | missense variant | G/A;C | snv | 1.8E-04; 8.2E-06 | 1 | ||
rs267606661 | 0.763 | 0.120 | 19 | 44909101 | missense variant | C/G;T | snv | 3.9E-04; 1.0E-05 | 10 | ||
rs28931576 | 19 | 44907894 | missense variant | A/G | snv | 1.2E-05 | 1.4E-05 | 1 | |||
rs121918393 | 0.851 | 0.120 | 19 | 44908756 | missense variant | C/A;T | snv | 1.3E-05; 9.0E-05 | 6 | ||
rs761592007 | 0.882 | 0.160 | 19 | 44909013 | missense variant | G/A | snv | 1.5E-05 | 4 | ||
rs121918396 | 1.000 | 0.080 | 19 | 44908979 | stop gained | G/A | snv | 1.6E-05 | 3.5E-05 | 1 | |
rs11542035 | 19 | 44908706 | missense variant | G/A | snv | 1.9E-05 | 2.8E-05 | 1 | |||
rs752600356 | 0.851 | 0.280 | 19 | 44908681 | missense variant | G/A;C | snv | 2.3E-05 | 1.4E-05 | 4 | |
rs28931578 | 19 | 44908751 | missense variant | G/A;C;T | snv | 3.2E-05 | 1 |