Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1800795 | 0.494 | 0.840 | 7 | 22727026 | intron variant | C/G | snv | 0.71 | 140 | ||
rs1333049 | 0.614 | 0.520 | 9 | 22125504 | intron variant | G/C | snv | 0.41 | 60 | ||
rs3813034 | 0.827 | 0.160 | 17 | 30197786 | 3 prime UTR variant | A/C | snv | 0.40 | 8 | ||
rs140701 | 0.790 | 0.200 | 17 | 30211514 | intron variant | C/T | snv | 0.40 | 7 | ||
rs4795541 | 0.807 | 0.200 | 17 | 30237299 | upstream gene variant | A/G | snv | 7 | |||
rs893051 | 0.807 | 0.400 | 3 | 190321812 | intron variant | G/A;C | snv | 7 | |||
rs17501010 | 0.827 | 0.320 | 3 | 190308865 | intron variant | G/T | snv | 0.15 | 5 | ||
rs117834366 | 0.925 | 0.120 | 7 | 147937799 | intron variant | G/A | snv | 1.2E-02 | 2 | ||
rs10491487 | 1.000 | 0.120 | 5 | 81027549 | intron variant | T/G | snv | 8.2E-02 | 1 | ||
rs12007229 | 1.000 | 0.120 | X | 67528513 | upstream gene variant | C/A | snv | 0.11 | 1 | ||
rs2497931 | 1.000 | 0.120 | X | 67436434 | intergenic variant | A/C;T | snv | 1 | |||
rs26906 | 1.000 | 0.120 | 5 | 81069068 | intron variant | T/C | snv | 0.86 | 1 | ||
rs290227 | 1.000 | 0.120 | 9 | 90874382 | intron variant | G/A | snv | 0.30 | 1 | ||
rs4485213 | 1.000 | 0.120 | 13 | 105256524 | intergenic variant | C/T | snv | 0.19 | 1 | ||
rs951660 | 1.000 | 0.120 | 3 | 111919285 | intron variant | A/C | snv | 0.86 | 1 | ||
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs1267969615 | 0.532 | 0.760 | 17 | 63490960 | missense variant | T/C | snv | 4.0E-06 | 100 | ||
rs769665945 | 0.882 | 0.160 | 7 | 101137079 | missense variant | C/A;T | snv | 4.0E-06; 3.6E-05 | 3 | ||
rs1051266 | 0.627 | 0.640 | 21 | 45537880 | missense variant | T/C;G | snv | 0.55; 4.4E-06 | 41 | ||
rs1800470 | 0.515 | 0.840 | 19 | 41353016 | missense variant | G/A;C | snv | 0.55; 2.4E-04 | 107 | ||
rs944050 | 0.827 | 0.280 | 14 | 64233327 | splice region variant | T/C | snv | 9.5E-02 | 7.9E-02 | 5 | |
rs429358 | 0.590 | 0.600 | 19 | 44908684 | missense variant | T/C | snv | 0.14 | 0.16 | 66 | |
rs4925 | 0.677 | 0.560 | 10 | 104263031 | missense variant | C/A | snv | 0.25 | 0.23 | 28 | |
rs7493 | 0.677 | 0.440 | 7 | 95405463 | missense variant | G/C | snv | 0.27 | 0.27 | 24 | |
rs854560 | 0.513 | 0.800 | 7 | 95316772 | missense variant | A/C;G;N;T | snv | 0.29 | 113 |