Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1057519723 | 0.925 | 0.120 | 9 | 5078362 | missense variant | A/C;G;T | snv | 1 | |||
rs1057519721 | 0.882 | 0.120 | 9 | 5078360 | missense variant | A/G | snv | 2 | |||
rs142269166 | 1.000 | 0.040 | 9 | 5126715 | missense variant | A/G | snv | 2.0E-03 | 2.1E-03 | 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 | ||
rs59384377 | 1.000 | 0.080 | 9 | 5005034 | intron variant | A/T | snv | 0.26 | 1 | ||
rs121912473 | 0.925 | 0.080 | 9 | 5070026 | missense variant | AA/TT | mnv | 2 | |||
rs7046736 | 0.925 | 0.080 | 9 | 5015732 | intron variant | C/A | snv | 0.39 | 2 | ||
rs12340895 | 1.000 | 0.080 | 9 | 5076691 | intron variant | C/A;G | snv | 1 | |||
rs771912975 | 1.000 | 0.040 | 9 | 5055750 | stop gained | C/A;G;T | snv | 4.0E-06; 1.6E-05 | 1 | ||
rs1057520016 | 0.851 | 0.080 | 9 | 5089726 | missense variant | C/A;T | snv | 4 | |||
rs10974944 | 0.882 | 0.160 | 9 | 5070831 | intron variant | C/G | snv | 0.25 | 4 | ||
rs1339159756 | 0.925 | 0.120 | 9 | 5078395 | missense variant | C/G | snv | 2 | |||
rs7849191 | 0.882 | 0.120 | 9 | 4988761 | intron variant | C/T | snv | 0.50 | 2 | ||
rs1319313254 | 9 | 5050807 | missense variant | C/T | snv | 4.0E-06 | 1 | ||||
rs3780378 | 1.000 | 0.040 | 9 | 5112288 | non coding transcript exon variant | C/T | snv | 0.51 | 1 | ||
rs2149556 | 1.000 | 0.080 | 9 | 5059440 | intron variant | C/T | snv | 0.64 | 1 | ||
rs2230724 | 0.851 | 0.120 | 9 | 5081780 | synonymous variant | G/A | snv | 0.53 | 0.62 | 4 | |
rs10974947 | 0.882 | 0.080 | 9 | 5072846 | intron variant | G/A | snv | 0.23 | 3 | ||
rs10815144 | 0.882 | 0.080 | 9 | 5010192 | intron variant | G/A | snv | 0.62 | 3 | ||
rs777015472 | 1.000 | 0.040 | 9 | 5066740 | missense variant | G/A | snv | 1.2E-05 | 7.0E-06 | 1 | |
rs1392759936 | 1.000 | 0.040 | 9 | 5054778 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
rs1346944271 | 1.000 | 0.120 | 9 | 5090497 | missense variant | G/A | snv | 1.4E-05 | 1 | ||
rs56118985 | 0.882 | 0.080 | 9 | 5044432 | missense variant | G/A;C | snv | 1.8E-03; 4.0E-06 | 3 | ||
rs774709145 | 9 | 5080657 | missense variant | G/A;C | snv | 1.3E-05 | 1 |