Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs9524885 | 13 | 95283335 | intron variant | T/C | snv | 0.63 | 2 | ||||
rs943552 | 1 | 156885826 | downstream gene variant | C/T | snv | 9.7E-02 | 2 | ||||
rs941601 | 14 | 94305204 | intron variant | C/T | snv | 0.19 | 1 | ||||
rs9340799 | 0.583 | 0.680 | 6 | 151842246 | intron variant | A/G | snv | 0.32 | 62 | ||
rs893924483 | 0.716 | 0.280 | 11 | 27658285 | missense variant | C/A;T | snv | 4.0E-06 | 1.4E-05 | 23 | |
rs8904 | 0.925 | 0.120 | 14 | 35402011 | 3 prime UTR variant | G/A;C;T | snv | 0.39; 4.0E-06 | 4 | ||
rs887200 | 22 | 19976143 | intron variant | C/T | snv | 0.74 | 1 | ||||
rs885479 | 0.732 | 0.280 | 16 | 89919746 | missense variant | G/A | snv | 0.15 | 8.3E-02 | 16 | |
rs879254102 | 2 | 166277257 | missense variant | C/T | snv | 1 | |||||
rs8136867 | 0.882 | 0.080 | 22 | 21850504 | intron variant | G/A | snv | 0.55 | 4 | ||
rs806378 | 1.000 | 0.040 | 6 | 88149832 | intron variant | C/T | snv | 0.21 | 2 | ||
rs80338958 | 0.790 | 0.200 | 17 | 63945614 | missense variant | C/A;T | snv | 1.6E-05; 5.6E-05 | 9 | ||
rs80338761 | 0.882 | 0.080 | 17 | 77402298 | missense variant | C/T | snv | 4 | |||
rs8007267 | 0.882 | 0.200 | 14 | 54912273 | intergenic variant | C/T | snv | 0.31 | 6 | ||
rs80026734 | 7 | 99676132 | missense variant | C/T | snv | 1 | |||||
rs796590326 | 0.851 | 0.200 | 12 | 121162449 | missense variant | GT/AC | mnv | 5 | |||
rs7958311 | 0.851 | 0.160 | 12 | 121167552 | missense variant | G/A;C | snv | 0.25; 4.0E-06 | 5 | ||
rs7824175 | 8 | 53231614 | intron variant | C/G;T | snv | 1 | |||||
rs781565158 | 0.851 | 0.120 | 12 | 21452130 | missense variant | A/G | snv | 4.7E-05 | 2.1E-05 | 22 | |
rs778056858 | 1.000 | 0.080 | 1 | 156866944 | missense variant | T/C | snv | 8.0E-06 | 7.0E-06 | 2 | |
rs7734804 | 5 | 164919530 | intron variant | G/T | snv | 8.3E-02 | 2 | ||||
rs773030005 | 1.000 | 0.040 | 4 | 69107204 | synonymous variant | A/C;G | snv | 4.0E-06; 6.8E-05 | 2 | ||
rs7718461 | 5 | 76962223 | intron variant | A/G | snv | 0.51 | 1 | ||||
rs77114424 | 6 | 154039497 | missense variant | G/A | snv | 2 | |||||
rs76992529 | 0.653 | 0.560 | 18 | 31598655 | missense variant | G/A | snv | 1.1E-03 | 4.9E-03 | 36 |