Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 25 | |
rs780094 | 0.658 | 0.400 | 2 | 27518370 | intron variant | T/C | snv | 0.67 | 24 | ||
rs653178 | 0.672 | 0.600 | 12 | 111569952 | intron variant | C/T | snv | 0.67 | 17 | ||
rs780093 | 0.763 | 0.240 | 2 | 27519736 | intron variant | T/C | snv | 0.68 | 13 | ||
rs8050136 | 0.716 | 0.560 | 16 | 53782363 | intron variant | C/A | snv | 0.40 | 11 | ||
rs17696736 | 0.827 | 0.240 | 12 | 112049014 | intron variant | A/G | snv | 0.30 | 11 | ||
rs671 | 0.529 | 0.840 | 12 | 111803962 | missense variant | G/A | snv | 1.9E-02 | 5.8E-03 | 10 | |
rs1260333 | 0.882 | 0.160 | 2 | 27525757 | downstream gene variant | A/G | snv | 0.58 | 8 | ||
rs1047891 | 0.827 | 0.200 | 2 | 210675783 | missense variant | C/A | snv | 0.30 | 0.33 | 8 | |
rs11066280 | 0.742 | 0.280 | 12 | 112379979 | intron variant | T/A | snv | 7.0E-03 | 8 | ||
rs3782886 | 0.724 | 0.480 | 12 | 111672685 | synonymous variant | T/C | snv | 1.9E-02 | 5.9E-03 | 7 | |
rs17145750 | 0.925 | 0.120 | 7 | 73612048 | intron variant | C/A;T | snv | 7 | |||
rs1169288 | 0.776 | 0.160 | 12 | 120978847 | missense variant | A/C;T | snv | 0.35 | 6 | ||
rs1051921 | 0.925 | 0.120 | 7 | 73593613 | 3 prime UTR variant | G/A | snv | 0.15 | 6 | ||
rs3823418 | 0.925 | 0.120 | 6 | 31133165 | intron variant | G/A | snv | 0.23 | 6 | ||
rs17145738 | 0.851 | 0.200 | 7 | 73568544 | 3 prime UTR variant | C/T | snv | 0.11 | 6 | ||
rs1150660 | 0.925 | 0.120 | 6 | 26101212 | upstream gene variant | A/C | snv | 0.73 | 5 | ||
rs199726 | 0.925 | 0.120 | 6 | 25953132 | intergenic variant | G/A | snv | 0.73 | 5 | ||
rs199734 | 0.925 | 0.120 | 6 | 25940165 | intergenic variant | G/A;C | snv | 5 | |||
rs199736 | 0.925 | 0.120 | 6 | 25936559 | intergenic variant | C/T | snv | 0.72 | 5 | ||
rs199737 | 0.925 | 0.120 | 6 | 25933310 | upstream gene variant | A/C;T | snv | 5 | |||
rs199739 | 0.925 | 0.120 | 6 | 25960281 | upstream gene variant | A/C;G | snv | 0.78 | 5 | ||
rs199751 | 0.925 | 0.120 | 6 | 26015355 | upstream gene variant | T/C | snv | 0.77 | 5 | ||
rs199752 | 0.925 | 0.120 | 6 | 26012647 | upstream gene variant | C/T | snv | 0.77 | 5 | ||
rs199753 | 0.925 | 0.120 | 6 | 26001660 | non coding transcript exon variant | G/A | snv | 0.77 | 5 |