Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs17782313 | 0.683 | 0.480 | 18 | 60183864 | intergenic variant | T/C | snv | 0.24 | 6 | ||
rs2001945 | 8 | 125465736 | upstream gene variant | G/A;C;T | snv | 6 | |||||
rs7138803 | 0.827 | 0.240 | 12 | 49853685 | intergenic variant | G/A;T | snv | 6 | |||
rs10938397 | 0.851 | 0.200 | 4 | 45180510 | intergenic variant | A/G | snv | 0.37 | 5 | ||
rs17700144 | 1.000 | 0.080 | 18 | 60144750 | intron variant | G/A | snv | 0.14 | 4 | ||
rs4854344 | 1.000 | 0.080 | 2 | 638144 | regulatory region variant | G/T | snv | 0.82 | 4 | ||
rs6548238 | 0.882 | 0.200 | 2 | 634905 | TF binding site variant | T/C | snv | 0.85 | 4 | ||
rs7561317 | 0.925 | 0.120 | 2 | 644953 | intergenic variant | A/G | snv | 0.81 | 4 | ||
rs998584 | 6 | 43790159 | downstream gene variant | C/A | snv | 0.41 | 4 | ||||
rs11084753 | 1.000 | 0.080 | 19 | 33831232 | intergenic variant | A/C;G;T | snv | 0.65 | 3 | ||
rs13141641 | 1.000 | 0.040 | 4 | 144585304 | intron variant | T/C | snv | 0.32 | 3 | ||
rs1394371 | 0.925 | 0.080 | 15 | 78432127 | intergenic variant | C/T | snv | 0.22 | 3 | ||
rs2036527 | 0.851 | 0.080 | 15 | 78559273 | regulatory region variant | G/A | snv | 0.29 | 3 | ||
rs2867125 | 0.925 | 0.120 | 2 | 622827 | intergenic variant | T/A;C | snv | 0.85 | 3 | ||
rs4887053 | 0.925 | 0.080 | 15 | 78420357 | regulatory region variant | A/C;T | snv | 3 | |||
rs10508503 | 1.000 | 0.080 | 10 | 16257952 | intergenic variant | C/A;T | snv | 2 | |||
rs1451240 | 0.925 | 0.080 | 8 | 42691568 | intergenic variant | A/G | snv | 0.64 | 2 | ||
rs1013443 | 5 | 180774114 | intergenic variant | A/T | snv | 1.4E-03 | 1 | ||||
rs10958725 | 8 | 42669441 | intergenic variant | T/G | snv | 0.63 | 1 | ||||
rs10958726 | 8 | 42680766 | intergenic variant | G/T | snv | 0.66 | 1 | ||||
rs11071927 | 15 | 66968834 | intergenic variant | C/A | snv | 0.85 | 1 | ||||
rs11205277 | 1.000 | 0.120 | 1 | 149920979 | upstream gene variant | A/C;G;T | snv | 1 | |||
rs12461383 | 19 | 40864433 | intron variant | C/G | snv | 0.42 | 1 | ||||
rs13273442 | 0.882 | 0.080 | 8 | 42688874 | intergenic variant | A/G | snv | 0.66 | 1 | ||
rs1383634 | 15 | 78737054 | downstream gene variant | T/C | snv | 0.53 | 1 |