Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs9275424 | 6 | 32702799 | downstream gene variant | A/G | snv | 0.30 | 1 | ||||
rs4293 | 17 | 63478305 | non coding transcript exon variant | G/A | snv | 0.45 | 1 | ||||
rs9896208 | 17 | 63498748 | intron variant | T/C | snv | 0.57 | 1 | ||||
rs11568054 | 1 | 230709809 | intron variant | G/A | snv | 3.6E-02 | 1 | ||||
rs7947841 | 11 | 34470133 | intron variant | G/A | snv | 1.0E-01 | 1 | ||||
rs55807605 | 1 | 196736919 | missense variant | G/A | snv | 1.4E-03 | 5.5E-04 | 1 | |||
rs57960694 | 1 | 196994083 | missense variant | G/A | snv | 1.1E-02 | 3.6E-02 | 1 | |||
rs1427118369 | 2 | 227283830 | missense variant | G/A | snv | 4.0E-06 | 1.4E-05 | 1 | |||
rs8731 | 2 | 27650459 | 3 prime UTR variant | C/G | snv | 0.22 | 1 | ||||
rs1317776692 | 14 | 104701619 | missense variant | C/G;T | snv | 4.4E-06 | 1 | ||||
rs17881180 | 21 | 31659974 | non coding transcript exon variant | C/T | snv | 3.8E-02 | 1 | ||||
rs9932581 | 16 | 88651945 | 3 prime UTR variant | C/T | snv | 0.39 | 1 | ||||
rs17880135 | 21 | 31669690 | upstream gene variant | T/G | snv | 3.9E-02 | 1 | ||||
rs204732 | 21 | 31720530 | intron variant | G/A | snv | 0.11 | 1 | ||||
rs10521145 | 16 | 28585563 | intron variant | G/A | snv | 0.11 | 1 | ||||
rs1025423410 | 4 | 38798831 | start lost | T/C | snv | 1 | |||||
rs776400293 | 4 | 186076620 | start lost | A/G | snv | 4.0E-06 | 7.0E-06 | 1 | |||
rs13293564 | 9 | 35166766 | intron variant | G/A;T | snv | 1 | |||||
rs2856717 | 1.000 | 0.120 | 6 | 32702531 | downstream gene variant | A/G | snv | 0.64 | 2 | ||
rs3115573 | 1.000 | 0.120 | 6 | 32251066 | upstream gene variant | A/G | snv | 0.41 | 2 | ||
rs6610650 | 1.000 | 0.040 | X | 37777261 | intron variant | G/A | snv | 0.27 | 2 | ||
rs11122576 | 1.000 | 0.080 | 1 | 230710933 | intron variant | T/C | snv | 8.2E-02 | 2 | ||
rs1926723 | 1.000 | 0.080 | 1 | 230704350 | intron variant | T/A;C;G | snv | 1.2E-05; 0.11; 2.0E-05 | 2 | ||
rs739401 | 11 | 3015094 | intron variant | C/T | snv | 0.45 | 2 | ||||
rs121912863 | 1.000 | 2 | 227008112 | missense variant | G/A | snv | 1.6E-04 | 1.8E-04 | 2 |