Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs9951307 | 0.882 | 0.120 | 18 | 26850565 | intron variant | G/A | snv | 0.65 | 5 | ||
rs899127658 | 0.547 | 0.720 | 11 | 46739084 | missense variant | G/A;C | snv | 82 | |||
rs8192597 | 1.000 | 0.040 | 18 | 907674 | synonymous variant | G/A | snv | 0.73 | 0.67 | 1 | |
rs80356779 | 0.776 | 0.320 | 11 | 68780662 | missense variant | G/A | snv | 3.2E-05 | 5.6E-05 | 10 | |
rs794728708 | 0.827 | 0.120 | 1 | 237377386 | missense variant | G/A;T | snv | 8 | |||
rs794728448 | 0.724 | 0.280 | 7 | 150948445 | frameshift variant | CT/G | delins | 17 | |||
rs786205867 | 0.882 | 0.080 | 1 | 111787039 | missense variant | C/T | snv | 3 | |||
rs77931234 | 0.925 | 0.120 | 1 | 75761161 | missense variant | A/C;G | snv | 3.3E-03 | 3 | ||
rs767910122 | 0.724 | 0.280 | 7 | 150948446 | frameshift variant | -/GTCCG | ins | 4.4E-05 | 17 | ||
rs7626962 | 0.790 | 0.080 | 3 | 38579416 | missense variant | G/A;T | snv | 1.6E-05; 5.9E-03 | 10 | ||
rs759834365 | 0.448 | 0.760 | 11 | 27658456 | missense variant | C/T | snv | 1.2E-05 | 237 | ||
rs758995 | 1.000 | 0.040 | 7 | 31064948 | intron variant | G/A | snv | 0.12 | 0.17 | 1 | |
rs757532106 | 0.763 | 0.120 | 3 | 38550500 | stop gained | G/A | snv | 4.5E-05 | 4.9E-05 | 9 | |
rs751377893 | 0.574 | 0.680 | 1 | 169546513 | missense variant | T/C | snv | 4.0E-06 | 65 | ||
rs72878794 | 1.000 | 0.040 | 18 | 26866839 | intron variant | C/A;T | snv | 8.1E-02 | 1 | ||
rs72552293 | 0.925 | 0.120 | 3 | 32140231 | missense variant | A/G | snv | 2.5E-03 | 2.9E-03 | 2 | |
rs72546668 | 0.807 | 0.200 | 3 | 8745644 | missense variant | C/A;T | snv | 4.0E-06; 2.6E-03 | 8 | ||
rs72466451 | 0.925 | 0.160 | 2 | 197498763 | missense variant | T/C | snv | 2 | |||
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 272 | |
rs4647924 | 0.600 | 0.520 | 4 | 1801844 | missense variant | C/A;G;T | snv | 4.2E-06; 4.2E-06 | 49 | ||
rs45546039 | 0.732 | 0.120 | 3 | 38613781 | missense variant | C/A;T | snv | 4.1E-06 | 15 | ||
rs3906956 | 1.000 | 0.040 | 18 | 26856350 | missense variant | A/G | snv | 1 | |||
rs368660364 | 1.000 | 0.040 | 20 | 33408748 | missense variant | C/T | snv | 1.6E-05 | 2.8E-05 | 1 | |
rs2856966 | 0.925 | 0.080 | 18 | 907709 | missense variant | A/G | snv | 0.19 | 0.18 | 2 | |
rs25531 | 0.581 | 0.520 | 17 | 30237328 | upstream gene variant | T/C | snv | 0.18 | 72 |