Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10132280 | 14 | 25458973 | intergenic variant | C/A | snv | 0.37 | 6 | ||||
rs10195252 | 0.925 | 0.080 | 2 | 164656581 | intron variant | T/C | snv | 0.48 | 6 | ||
rs10804591 | 3 | 129615390 | intergenic variant | C/A | snv | 0.63 | 4 | ||||
rs10842707 | 12 | 26318431 | intron variant | C/G;T | snv | 4 | |||||
rs10919388 | 1 | 170403362 | intergenic variant | A/C | snv | 0.71 | 4 | ||||
rs10923712 | 1 | 118962811 | intron variant | G/A | snv | 0.56 | 4 | ||||
rs10938397 | 0.851 | 0.200 | 4 | 45180510 | intergenic variant | A/G | snv | 0.37 | 8 | ||
rs1167827 | 7 | 75533848 | 3 prime UTR variant | G/A | snv | 0.37 | 5 | ||||
rs12317176 | 12 | 123920171 | intron variant | T/C | snv | 0.39 | 3 | ||||
rs12429545 | 13 | 53528071 | intron variant | G/A;T | snv | 0.12 | 4 | ||||
rs12446632 | 1.000 | 0.080 | 16 | 19924067 | intergenic variant | G/A | snv | 0.11 | 7 | ||
rs12493901 | 3 | 172204265 | intron variant | G/A | snv | 0.37 | 3 | ||||
rs12731372 | 1 | 118310352 | regulatory region variant | C/T | snv | 0.19 | 3 | ||||
rs12885454 | 14 | 29267632 | non coding transcript exon variant | C/A | snv | 0.27 | 4 | ||||
rs12991495 | 2 | 25263901 | intron variant | T/C | snv | 0.22 | 3 | ||||
rs13083798 | 3 | 52615732 | intron variant | A/G | snv | 0.51 | 3 | ||||
rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 24 | ||
rs13191362 | 6 | 162612318 | intron variant | A/G | snv | 8.7E-02 | 3 | ||||
rs1358980 | 6 | 43796814 | intergenic variant | C/T | snv | 0.40 | 6 | ||||
rs1443512 | 12 | 53948900 | downstream gene variant | A/C;T | snv | 4 | |||||
rs17024393 | 1 | 109612066 | intron variant | T/C | snv | 4.6E-02 | 4 | ||||
rs17405819 | 8 | 75894349 | intergenic variant | T/C | snv | 0.24 | 3 | ||||
rs17451107 | 3 | 157079820 | upstream gene variant | T/C | snv | 0.38 | 7 | ||||
rs17819328 | 3 | 12447843 | intergenic variant | T/A;G | snv | 4 | |||||
rs1812175 | 4 | 144653692 | intron variant | A/G | snv | 0.79 | 5 |