Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs998584 | 6 | 43790159 | downstream gene variant | C/A | snv | 0.41 | 11 | ||||
rs3810291 | 19 | 47065746 | 3 prime UTR variant | G/A | snv | 0.50 | 9 | ||||
rs2145272 | 20 | 6645571 | intergenic variant | G/A;T | snv | 8 | |||||
rs17451107 | 3 | 157079820 | upstream gene variant | T/C | snv | 0.38 | 7 | ||||
rs10132280 | 14 | 25458973 | intergenic variant | C/A | snv | 0.37 | 6 | ||||
rs10408163 | 19 | 47093845 | non coding transcript exon variant | T/C | snv | 0.52 | 6 | ||||
rs1358980 | 6 | 43796814 | intergenic variant | C/T | snv | 0.40 | 6 | ||||
rs1812175 | 4 | 144653692 | intron variant | A/G | snv | 0.79 | 6 | ||||
rs395962 | 6 | 104949543 | intron variant | T/G | snv | 0.72 | 6 | ||||
rs55872725 | 16 | 53775211 | intron variant | C/T | snv | 0.31 | 6 | ||||
rs7133378 | 12 | 123924955 | intron variant | G/A | snv | 0.38 | 6 | ||||
rs806794 | 6 | 26200449 | 3 prime UTR variant | A/G | snv | 0.36 | 6 | ||||
rs10804591 | 3 | 129615390 | intergenic variant | C/A | snv | 0.63 | 5 | ||||
rs11672660 | 19 | 45676926 | intron variant | C/T | snv | 0.18 | 0.17 | 5 | |||
rs1167827 | 7 | 75533848 | 3 prime UTR variant | G/A | snv | 0.37 | 5 | ||||
rs1884897 | 20 | 6632185 | regulatory region variant | A/G;T | snv | 5 | |||||
rs2274432 | 1 | 184051811 | missense variant | G/A | snv | 0.33 | 0.28 | 5 | |||
rs2371767 | 3 | 64732582 | intron variant | G/C | snv | 0.38 | 5 | ||||
rs2650492 | 16 | 28322090 | 3 prime UTR variant | G/A | snv | 0.20 | 5 | ||||
rs4823006 | 22 | 29055683 | 3 prime UTR variant | A/G | snv | 0.41 | 5 | ||||
rs4896582 | 6 | 142382740 | intron variant | G/A | snv | 0.50 | 5 | ||||
rs6556301 | 5 | 177100576 | downstream gene variant | G/T | snv | 0.33 | 5 | ||||
rs7536458 | 1 | 118321979 | intergenic variant | T/G | snv | 0.23 | 5 | ||||
rs7801581 | 7 | 27184152 | intron variant | C/T | snv | 0.24 | 5 | ||||
rs10842707 | 12 | 26318431 | intron variant | C/G;T | snv | 4 |