Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs998731 | 1.000 | 0.120 | 8 | 80183160 | intron variant | C/G;T | snv | 1 | |||
rs9979383 | 0.925 | 0.200 | 21 | 35343463 | intron variant | C/G;T | snv | 5 | |||
rs991760 | 1.000 | 0.120 | 6 | 32855790 | intron variant | G/A | snv | 8.2E-02 | 1 | ||
rs9909240 | 1.000 | 0.120 | 17 | 9236774 | intron variant | G/A | snv | 0.50 | 1 | ||
rs9880772 | 0.827 | 0.240 | 3 | 27736288 | intergenic variant | G/A | snv | 0.59 | 5 | ||
rs987870 | 0.851 | 0.160 | 6 | 33075103 | intron variant | A/G | snv | 0.19 | 3 | ||
rs986521 | 1.000 | 0.120 | 6 | 33168368 | intron variant | G/A;C | snv | 1 | |||
rs9860428 | 1.000 | 0.120 | 3 | 112852072 | intergenic variant | C/A;G;T | snv | 1 | |||
rs984778 | 1.000 | 0.120 | 6 | 32432311 | TF binding site variant | C/T | snv | 0.62 | 1 | ||
rs983561 | 1.000 | 0.120 | 6 | 32435878 | upstream gene variant | T/C;G | snv | 1 | |||
rs9826828 | 1.000 | 0.120 | 3 | 136683218 | intron variant | G/A | snv | 1.3E-02 | 1 | ||
rs9785133 | 1.000 | 0.120 | 8 | 20501107 | intergenic variant | C/T | snv | 0.21 | 1 | ||
rs9784876 | 1.000 | 0.120 | 6 | 32821101 | intron variant | C/A | snv | 0.11 | 1 | ||
rs9784858 | 0.925 | 0.200 | 6 | 32819398 | intron variant | G/C | snv | 0.12 | 2 | ||
rs9784758 | 0.925 | 0.200 | 6 | 32820734 | intron variant | T/C | snv | 0.11 | 2 | ||
rs969891 | 1.000 | 0.120 | 6 | 32348638 | intron variant | T/C;G | snv | 1 | |||
rs968567 | 0.851 | 0.240 | 11 | 61828092 | intron variant | C/T | snv | 0.11 | 6 | ||
rs9653442 | 1.000 | 0.120 | 2 | 100208905 | intron variant | C/T | snv | 0.46 | 2 | ||
rs964184 | 0.716 | 0.440 | 11 | 116778201 | 3 prime UTR variant | G/C | snv | 0.82 | 38 | ||
rs9635 | 1.000 | 0.120 | 11 | 33079306 | non coding transcript exon variant | C/T | snv | 1 | |||
rs9604529 | 1.000 | 0.120 | 13 | 113919624 | non coding transcript exon variant | A/G;T | snv | 0.17; 7.4E-06 | 1 | ||
rs9603618 | 1.000 | 0.120 | 13 | 39797240 | intergenic variant | C/T | snv | 0.24 | 1 | ||
rs9603616 | 1.000 | 0.120 | 13 | 39793932 | downstream gene variant | C/T | snv | 0.30 | 1 | ||
rs9603612 | 0.925 | 0.120 | 13 | 39760715 | intron variant | C/G | snv | 0.30 | 2 | ||
rs9598783 | 1.000 | 0.120 | 13 | 64371042 | TF binding site variant | C/G | snv | 0.43 | 1 |