Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2283847 | 22 | 27785411 | intron variant | C/A;G;T | snv | 7 | |||||
rs2112347 | 0.925 | 0.120 | 5 | 75719417 | upstream gene variant | T/G | snv | 0.42 | 7 | ||
rs11694173 | 0.827 | 0.080 | 2 | 43363760 | intron variant | G/A | snv | 0.14 | 7 | ||
rs863750 | 12 | 124020897 | intron variant | C/T | snv | 0.53 | 7 | ||||
rs10132280 | 14 | 25458973 | intergenic variant | C/A | snv | 0.37 | 6 | ||||
rs10808546 | 8 | 125483576 | intron variant | C/T | snv | 0.39 | 6 | ||||
rs645040 | 3 | 136207780 | upstream gene variant | G/T | snv | 0.77 | 6 | ||||
rs1800978 | 1.000 | 0.040 | 9 | 104903697 | 5 prime UTR variant | C/A;G;T | snv | 5.4E-06; 0.14 | 6 | ||
rs1883025 | 0.807 | 0.120 | 9 | 104902020 | intron variant | C/T | snv | 0.28 | 6 | ||
rs6795735 | 0.882 | 0.120 | 3 | 64719689 | intron variant | C/A;G;T | snv | 6 | |||
rs10195252 | 0.925 | 0.080 | 2 | 164656581 | intron variant | T/C | snv | 0.48 | 6 | ||
rs13101828 | 0.851 | 0.160 | 4 | 971932 | intron variant | A/G | snv | 0.43 | 6 | ||
rs7133378 | 12 | 123924955 | intron variant | G/A | snv | 0.38 | 6 | ||||
rs1358980 | 6 | 43796814 | intergenic variant | C/T | snv | 0.40 | 6 | ||||
rs1142 | 0.851 | 0.040 | 7 | 105115879 | intron variant | C/T | snv | 0.31 | 6 | ||
rs13130484 | 1.000 | 0.080 | 4 | 45173674 | intergenic variant | C/A;T | snv | 5 | |||
rs62106258 | 1.000 | 0.040 | 2 | 417167 | upstream gene variant | T/C | snv | 2.9E-02 | 5 | ||
rs6556301 | 5 | 177100576 | downstream gene variant | G/T | snv | 0.33 | 5 | ||||
rs727428 | 0.882 | 0.200 | 17 | 7634474 | downstream gene variant | T/C | snv | 0.55 | 5 | ||
rs7536458 | 1 | 118321979 | intergenic variant | T/G | snv | 0.23 | 5 | ||||
rs979012 | 1.000 | 0.080 | 20 | 6642727 | intergenic variant | T/C | snv | 0.67 | 5 | ||
rs2371767 | 3 | 64732582 | intron variant | G/C | snv | 0.38 | 5 | ||||
rs2278426 | 1.000 | 0.080 | 19 | 11239812 | missense variant | C/T | snv | 0.11 | 0.11 | 5 | |
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 5 | |
rs13389219 | 1.000 | 0.080 | 2 | 164672366 | intron variant | C/T | snv | 0.47 | 5 |