Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4291 | 0.724 | 0.400 | 17 | 63476833 | upstream gene variant | T/A;C | snv | 1 | |||
rs2710102 | 0.790 | 0.120 | 7 | 147877298 | intron variant | A/G;T | snv | 1 | |||
rs6740584 | 0.882 | 0.040 | 2 | 207564627 | intron variant | T/C | snv | 0.37 | 1 | ||
rs1360780 | 0.708 | 0.320 | 6 | 35639794 | intron variant | T/A;C | snv | 1 | |||
rs1488864 | 0.851 | 0.080 | 11 | 6321099 | intron variant | T/G | snv | 0.80 | 1 | ||
rs1545843 | 0.827 | 0.120 | 12 | 84170289 | intron variant | G/A | snv | 0.52 | 1 | ||
rs760161369 | 0.882 | 0.040 | 1 | 11800214 | missense variant | G/A;C | snv | 2.8E-05; 4.0E-06 | 1 | ||
rs4512342 | 0.827 | 0.120 | 8 | 32750356 | intron variant | T/G | snv | 0.12 | 1 | ||
rs2522833 | 0.827 | 0.080 | 7 | 82824392 | missense variant | A/C | snv | 0.45 | 0.34 | 1 | |
rs2984618 | 0.925 | 0.040 | 1 | 47224766 | intron variant | G/T | snv | 0.52 | 1 | ||
rs10514299 | 0.827 | 0.120 | 5 | 88367793 | intron variant | C/T | snv | 0.21 | 1 | ||
rs120074175 | 0.827 | 0.080 | 12 | 72031544 | missense variant | G/A | snv | 1.2E-05 | 7.0E-06 | 1 | |
rs2228570 | 0.521 | 0.760 | 12 | 47879112 | start lost | A/C;G;T | snv | 0.63 | 1 | ||
rs1344706 | 0.701 | 0.160 | 2 | 184913701 | intron variant | A/C;T | snv | 1 | |||
rs10233018 | 0.925 | 0.040 | 7 | 117883655 | non coding transcript exon variant | A/G | snv | 0.53 | 2 | ||
rs10485715 | 0.925 | 0.040 | 20 | 7279278 | intergenic variant | T/C | snv | 5.5E-02 | 2 | ||
rs10809520 | 0.925 | 0.040 | 9 | 11557797 | intergenic variant | C/T | snv | 0.28 | 2 | ||
rs4685959 | 0.925 | 0.040 | 3 | 5645577 | regulatory region variant | C/G;T | snv | 2 | |||
rs4810896 | 0.925 | 0.040 | 20 | 48918761 | upstream gene variant | A/C;G | snv | 2 | |||
rs75921243 | 0.925 | 0.040 | 8 | 9988356 | intron variant | T/G | snv | 1.9E-02 | 2 | ||
rs76767803 | 0.925 | 0.040 | 3 | 36230378 | intergenic variant | C/T | snv | 0.16 | 2 | ||
rs10994336 | 0.776 | 0.160 | 10 | 60420054 | intron variant | C/T | snv | 7.5E-02 | 2 | ||
rs116609693 | 0.925 | 0.040 | 9 | 92811394 | intron variant | C/T | snv | 6.1E-02 | 2 | ||
rs1401635 | 0.925 | 0.040 | 11 | 27672444 | intron variant | C/G | snv | 0.73 | 2 | ||
rs1961982 | 0.925 | 0.040 | 12 | 103218955 | intergenic variant | G/A | snv | 0.27 | 2 |