Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11166389 | 1.000 | 0.040 | 1 | 100000723 | non coding transcript exon variant | G/A | snv | 0.15 | 2 | ||
rs12021720 | 0.925 | 0.160 | 1 | 100206504 | missense variant | T/A;C | snv | 0.92 | 3 | ||
rs10165970 | 0.708 | 0.320 | 2 | 100840527 | intron variant | G/A | snv | 0.16 | 18 | ||
rs17024869 | 0.708 | 0.320 | 2 | 100843581 | intron variant | T/C | snv | 8.3E-02 | 18 | ||
rs895520 | 0.689 | 0.320 | 2 | 100961475 | intron variant | G/A | snv | 0.35 | 23 | ||
rs7581886 | 0.708 | 0.320 | 2 | 100964784 | intron variant | C/T | snv | 0.92 | 18 | ||
rs782414948 | 1.000 | 0.040 | 7 | 102227624 | missense variant | G/A | snv | 3.2E-05 | 2.8E-05 | 1 | |
rs749124997 | 1.000 | 0.040 | 12 | 102402539 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
rs1799969 | 0.637 | 0.560 | 19 | 10284116 | missense variant | G/A | snv | 0.11 | 9.3E-02 | 38 | |
rs17655 | 0.597 | 0.560 | 13 | 102875652 | missense variant | G/C | snv | 0.28 | 0.30 | 52 | |
rs3212112 | 1.000 | 0.040 | 14 | 103699345 | intron variant | A/C | snv | 7.1E-03 | 2.2E-02 | 1 | |
rs861539 | 0.519 | 0.680 | 14 | 103699416 | missense variant | G/A | snv | 0.29 | 0.30 | 104 | |
rs11598018 | 1.000 | 0.040 | 10 | 103901557 | intron variant | C/A;T | snv | 2 | |||
rs71305152 | 0.882 | 0.040 | 8 | 105437494 | intron variant | -/TTTTCT | delins | 0.43 | 5 | ||
rs3851634 | 0.882 | 0.040 | 12 | 106419124 | intron variant | T/C | snv | 0.22 | 4 | ||
rs1273593548 | 0.716 | 0.160 | 7 | 106867593 | missense variant | T/G | snv | 8.4E-06 | 19 | ||
rs10494090 | 1.000 | 0.040 | 1 | 108150714 | intron variant | A/C;G;T | snv | 2 | |||
rs10131 | 1.000 | 0.040 | 13 | 108207498 | 3 prime UTR variant | C/T | snv | 0.12 | 3 | ||
rs1805388 | 0.790 | 0.120 | 13 | 108211243 | missense variant | G/A | snv | 0.18 | 0.16 | 11 | |
rs3093739 | 1.000 | 0.040 | 13 | 108215053 | intron variant | A/G | snv | 8.8E-02 | 1 | ||
rs3092993 | 0.827 | 0.040 | 11 | 108364388 | intron variant | C/A | snv | 0.11 | 5 | ||
rs3787016 | 0.677 | 0.280 | 19 | 1090804 | intron variant | A/G | snv | 0.78 | 24 | ||
rs4845964 | 1.000 | 0.040 | 1 | 10920487 | regulatory region variant | G/A | snv | 0.36 | 2 | ||
rs4444903 | 0.630 | 0.360 | 4 | 109912954 | 5 prime UTR variant | A/G | snv | 0.51 | 35 | ||
rs776728511 | 0.925 | 0.040 | 4 | 109945192 | missense variant | A/G | snv | 4.0E-06 | 2 |