Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs899127658 | 0.547 | 0.720 | 11 | 46739084 | missense variant | G/A;C | snv | 82 | |||
rs25531 | 0.581 | 0.520 | 17 | 30237328 | upstream gene variant | T/C | snv | 0.18 | 72 | ||
rs2069705 | 0.695 | 0.440 | 12 | 68161231 | intron variant | G/A;C | snv | 19 | |||
rs767910122 | 0.724 | 0.280 | 7 | 150948446 | frameshift variant | -/GTCCG | ins | 4.4E-05 | 17 | ||
rs794728448 | 0.724 | 0.280 | 7 | 150948445 | frameshift variant | CT/G | delins | 17 | |||
rs2069718 | 0.742 | 0.320 | 12 | 68156382 | intron variant | A/G;T | snv | 0.50 | 14 | ||
rs1318358361 | 0.724 | 0.240 | 6 | 156778678 | missense variant | C/G | snv | 2.1E-05 | 13 | ||
rs2069727 | 0.763 | 0.320 | 12 | 68154443 | intron variant | T/A;C | snv | 9 | |||
rs794728708 | 0.827 | 0.120 | 1 | 237377386 | missense variant | G/A;T | snv | 8 | |||
rs10494366 | 0.851 | 0.200 | 1 | 162115895 | intron variant | G/T | snv | 0.54 | 7 | ||
rs2075575 | 0.851 | 0.200 | 18 | 26866562 | intron variant | G/A | snv | 0.31 | 5 | ||
rs9951307 | 0.882 | 0.120 | 18 | 26850565 | intron variant | G/A | snv | 0.65 | 5 | ||
rs199473604 | 0.882 | 0.120 | 3 | 38560394 | missense variant | G/T | snv | 4 | |||
rs786205867 | 0.882 | 0.080 | 1 | 111787039 | missense variant | C/T | snv | 3 | |||
rs1064795287 | 0.925 | 0.120 | 7 | 150947683 | frameshift variant | GG/T | delins | 2 | |||
rs12133079 | 1.000 | 0.040 | 1 | 160046674 | intron variant | C/A | snv | 0.13 | 2 | ||
rs121909282 | 0.925 | 0.120 | 3 | 8745647 | missense variant | T/G | snv | 1.4E-05 | 2 | ||
rs1361625573 | 0.925 | 0.080 | 5 | 474979 | missense variant | A/G | snv | 7.0E-06 | 2 | ||
rs1893154 | 0.925 | 0.080 | 18 | 905124 | 5 prime UTR variant | A/G | snv | 0.72 | 2 | ||
rs199473014 | 0.925 | 0.120 | 7 | 150947684 | missense variant | G/T | snv | 2.1E-05 | 2 | ||
rs72466451 | 0.925 | 0.160 | 2 | 197498763 | missense variant | T/C | snv | 2 | |||
rs10081254 | 1.000 | 0.040 | 7 | 31082056 | intron variant | C/T | snv | 0.12 | 1 | ||
rs1178561476 | 1.000 | 0.040 | 1 | 111777204 | missense variant | A/G | snv | 1 | |||
rs1186688 | 1.000 | 0.040 | 1 | 160055093 | intron variant | T/C | snv | 0.41 | 1 | ||
rs17375748 | 1.000 | 0.040 | 1 | 160040361 | 3 prime UTR variant | C/G;T | snv | 1 |