Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10750097 | 1.000 | 0.040 | 11 | 116793324 | upstream gene variant | G/A;C | snv | 6 | |||
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 81 | |
rs1263173 | 0.925 | 0.080 | 11 | 116810292 | downstream gene variant | G/A | snv | 0.53 | 4 | ||
rs13702 | 0.925 | 0.160 | 8 | 19966981 | 3 prime UTR variant | T/A;C | snv | 7 | |||
rs16996148 | 0.882 | 0.120 | 19 | 19547663 | downstream gene variant | G/T | snv | 0.10 | 8 | ||
rs17321515 | 0.776 | 0.200 | 8 | 125474167 | intron variant | A/G | snv | 0.49 | 16 | ||
rs2228603 | 0.790 | 0.360 | 19 | 19219115 | missense variant | C/A;T | snv | 2.8E-05; 5.9E-02 | 12 | ||
rs268 | 0.637 | 0.480 | 8 | 19956018 | missense variant | A/G | snv | 1.3E-02 | 1.3E-02 | 41 | |
rs2954021 | 1.000 | 0.040 | 8 | 125469835 | intron variant | A/G | snv | 0.54 | 15 | ||
rs2954029 | 0.807 | 0.160 | 8 | 125478730 | intron variant | A/T | snv | 0.42 | 14 | ||
rs2980888 | 1.000 | 0.040 | 8 | 125495066 | intron variant | T/C | snv | 0.76 | 2 | ||
rs3135507 | 0.925 | 0.120 | 11 | 116790772 | missense variant | C/T | snv | 5.0E-02 | 5.5E-02 | 3 | |
rs328 | 0.732 | 0.440 | 8 | 19962213 | stop gained | C/G | snv | 9.2E-02 | 9.0E-02 | 19 | |
rs4808199 | 1.000 | 0.040 | 19 | 19434290 | intron variant | G/A;T | snv | 0.19 | 5 | ||
rs58542926 | 0.630 | 0.440 | 19 | 19268740 | missense variant | C/T | snv | 6.5E-02 | 5.8E-02 | 42 | |
rs662799 | 0.689 | 0.480 | 11 | 116792991 | upstream gene variant | G/A | snv | 0.90 | 33 | ||
rs780094 | 0.658 | 0.400 | 2 | 27518370 | intron variant | T/C | snv | 0.67 | 62 | ||
rs7946 | 0.851 | 0.160 | 17 | 17506246 | missense variant | C/T | snv | 0.59 | 0.59 | 6 | |
rs9939609 | 0.559 | 0.720 | 16 | 53786615 | intron variant | T/A | snv | 0.41 | 98 |