Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12343867 | 0.790 | 0.200 | 9 | 5074189 | intron variant | T/C | snv | 0.25 | 9 | ||
rs12342421 | 0.851 | 0.080 | 9 | 5065750 | intron variant | G/C | snv | 0.23 | 4 | ||
rs10974944 | 0.882 | 0.160 | 9 | 5070831 | intron variant | C/G | snv | 0.25 | 4 | ||
rs1057520016 | 0.851 | 0.080 | 9 | 5089726 | missense variant | C/A;T | snv | 4 | |||
rs10974947 | 0.882 | 0.080 | 9 | 5072846 | intron variant | G/A | snv | 0.23 | 3 | ||
rs10815148 | 0.882 | 0.080 | 9 | 5057284 | intron variant | T/A | snv | 0.33 | 3 | ||
rs10815144 | 0.882 | 0.080 | 9 | 5010192 | intron variant | G/A | snv | 0.62 | 3 | ||
rs12349785 | 0.882 | 0.080 | 9 | 5076613 | intron variant | G/C | snv | 0.23 | 3 | ||
rs4495487 | 0.925 | 0.080 | 9 | 5072798 | intron variant | T/C | snv | 0.23 | 3 | ||
rs1339159756 | 0.925 | 0.120 | 9 | 5078395 | missense variant | C/G | snv | 2 | |||
rs121912472 | 0.925 | 0.080 | 9 | 5073742 | missense variant | G/C | snv | 2 | |||
rs121912473 | 0.925 | 0.080 | 9 | 5070026 | missense variant | AA/TT | mnv | 2 | |||
rs12339666 | 0.925 | 0.080 | 9 | 5063296 | intron variant | G/T | snv | 0.34 | 2 | ||
rs7046736 | 0.925 | 0.080 | 9 | 5015732 | intron variant | C/A | snv | 0.39 | 2 | ||
rs3808850 | 0.925 | 0.080 | 9 | 4983311 | upstream gene variant | T/A;C | snv | 2 | |||
rs7849191 | 0.882 | 0.120 | 9 | 4988761 | intron variant | C/T | snv | 0.50 | 2 | ||
rs7857730 | 0.925 | 0.040 | 9 | 5084049 | intron variant | G/A;T | snv | 0.63 | 2 | ||
rs1057519721 | 0.882 | 0.120 | 9 | 5078360 | missense variant | A/G | snv | 2 | |||
rs1159782 | 1.000 | 0.040 | 9 | 5078117 | intron variant | T/C | snv | 0.23 | 1 | ||
rs923941004 | 1.000 | 0.040 | 9 | 5078334 | missense variant | T/C | snv | 1 | |||
rs1392759936 | 1.000 | 0.040 | 9 | 5054778 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
rs1479478620 | 1.000 | 0.040 | 9 | 5126768 | missense variant | A/G | snv | 1 | |||
rs2274471 | 1.000 | 0.040 | 9 | 4985879 | intron variant | A/G | snv | 0.21 | 1 | ||
rs3780378 | 1.000 | 0.040 | 9 | 5112288 | non coding transcript exon variant | C/T | snv | 0.51 | 1 | ||
rs1346944271 | 1.000 | 0.120 | 9 | 5090497 | missense variant | G/A | snv | 1.4E-05 | 1 |