Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs9468 | 0.882 | 0.080 | 17 | 46024197 | 3 prime UTR variant | T/C | snv | 0.15 | 0.14 | 6 | |
rs943437 | 1.000 | 0.040 | 6 | 111921050 | regulatory region variant | A/G | snv | 0.30 | 1 | ||
rs9347683 | 0.882 | 0.120 | 6 | 162728023 | 5 prime UTR variant | A/C;G | snv | 3 | |||
rs9340799 | 0.583 | 0.680 | 6 | 151842246 | intron variant | A/G | snv | 0.32 | 62 | ||
rs932546861 | 1.000 | 0.040 | 4 | 99347032 | frameshift variant | C/- | delins | 1 | |||
rs9323124 | 0.925 | 0.040 | 14 | 46996974 | non coding transcript exon variant | T/A | snv | 0.23 | 2 | ||
rs9275326 | 1.000 | 0.040 | 6 | 32698883 | intergenic variant | C/T | snv | 9.1E-02 | 1 | ||
rs9268515 | 1.000 | 0.040 | 6 | 32411518 | upstream gene variant | G/C | snv | 0.16 | 1 | ||
rs921420972 | 1.000 | 0.040 | 15 | 48610824 | missense variant | T/C | snv | 2.1E-05 | 1 | ||
rs914722 | 1.000 | 0.040 | 1 | 54048154 | intron variant | T/A;C | snv | 1 | |||
rs906807 | 1.000 | 0.040 | 18 | 9117869 | missense variant | T/C;G | snv | 0.80; 4.0E-06 | 1 | ||
rs897984 | 0.925 | 0.080 | 16 | 30875322 | non coding transcript exon variant | T/C | snv | 0.62 | 0.47 | 2 | |
rs894278 | 0.882 | 0.080 | 4 | 89813384 | intron variant | T/G | snv | 0.15 | 4 | ||
rs893924483 | 0.716 | 0.280 | 11 | 27658285 | missense variant | C/A;T | snv | 4.0E-06 | 1.4E-05 | 23 | |
rs892145 | 1.000 | 0.040 | 19 | 15475861 | missense variant | A/T | snv | 0.36 | 0.38 | 2 | |
rs886042808 | 1.000 | 0.040 | 6 | 41161481 | missense variant | C/G;T | snv | 4.0E-06 | 1 | ||
rs885479 | 0.732 | 0.280 | 16 | 89919746 | missense variant | G/A | snv | 0.15 | 8.3E-02 | 16 | |
rs879253853 | 1.000 | 0.040 | 15 | 62013057 | frameshift variant | -/TCTG | ins | 1 | |||
rs878888 | 1.000 | 0.040 | 17 | 45835269 | 3 prime UTR variant | A/G | snv | 0.14 | 1 | ||
rs878887 | 1.000 | 0.040 | 17 | 45835216 | 3 prime UTR variant | C/T | snv | 0.14 | 2 | ||
rs878886 | 0.925 | 0.080 | 17 | 45835124 | 3 prime UTR variant | C/G;T | snv | 3 | |||
rs876658902 | 0.925 | 0.040 | 17 | 7676182 | missense variant | C/T | snv | 3 | |||
rs875989836 | 0.925 | 0.160 | 11 | 6394384 | missense variant | T/C | snv | 2 | |||
rs870575 | 1.000 | 0.040 | 2 | 45276121 | intron variant | G/A;C | snv | 1 | |||
rs869312811 | 0.925 | 0.040 | 15 | 61947292 | frameshift variant | G/- | delins | 2 |