Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs9340799 | 0.583 | 0.680 | 6 | 151842246 | intron variant | A/G | snv | 0.32 | 62 | ||
rs1800797 | 0.605 | 0.800 | 7 | 22726602 | non coding transcript exon variant | A/G | snv | 0.72 | 43 | ||
rs1800682 | 0.637 | 0.440 | 10 | 88990206 | non coding transcript exon variant | A/G | snv | 0.54 | 32 | ||
rs6746030 | 0.763 | 0.320 | 2 | 166242648 | missense variant | A/G | snv | 0.88 | 0.88 | 16 | |
rs121913474 | 0.790 | 0.200 | 10 | 121515260 | missense variant | A/G | snv | 9 | |||
rs16901946 | 0.827 | 0.160 | 8 | 127088680 | non coding transcript exon variant | A/G | snv | 1.7E-02 | 8 | ||
rs2073711 | 0.807 | 0.160 | 15 | 65201874 | missense variant | A/G | snv | 0.56 | 0.61 | 7 | |
rs5030772 | 0.790 | 0.320 | 1 | 172664210 | intron variant | A/G | snv | 9.9E-02 | 7 | ||
rs121918505 | 0.851 | 0.080 | 10 | 121520119 | missense variant | A/G | snv | 5 | |||
rs904571820 | 0.851 | 0.160 | 6 | 151842664 | start lost | A/G | snv | 4.0E-06 | 5 | ||
rs10948172 | 0.882 | 0.040 | 6 | 44809954 | intron variant | A/G | snv | 0.27 | 3 | ||
rs12901071 | 0.882 | 0.160 | 15 | 67078051 | intron variant | A/G | snv | 0.25 | 3 | ||
rs1800802 | 0.925 | 0.040 | 12 | 14885985 | intron variant | A/G | snv | 0.15 | 3 | ||
rs226794 | 0.882 | 0.160 | 21 | 26930036 | missense variant | A/G | snv | 0.83 | 0.89 | 3 | |
rs1044122 | 0.925 | 0.040 | 10 | 126036209 | synonymous variant | A/G | snv | 0.27 | 0.26 | 2 | |
rs11564299 | 0.925 | 0.040 | 18 | 28180064 | upstream gene variant | A/G | snv | 0.17 | 2 | ||
rs13301537 | 0.925 | 0.040 | 9 | 92466765 | intron variant | A/G | snv | 0.38 | 2 | ||
rs1913707 | 0.925 | 0.040 | 4 | 13037816 | intergenic variant | A/G | snv | 0.40 | 2 | ||
rs3771501 | 0.925 | 0.040 | 2 | 70490521 | intron variant | A/G | snv | 0.60 | 2 | ||
rs520540 | 0.925 | 0.120 | 11 | 102838694 | synonymous variant | A/G | snv | 0.57 | 0.54 | 2 | |
rs835487 | 0.925 | 0.040 | 12 | 104666989 | intron variant | A/G | snv | 0.43 | 2 | ||
rs912428 | 0.925 | 0.040 | 13 | 46593768 | intron variant | A/G | snv | 0.84 | 2 | ||
rs116855380 | 1.000 | 0.040 | 20 | 47491550 | downstream gene variant | A/G | snv | 2.8E-02 | 1 | ||
rs11688000 | 1.000 | 0.040 | 2 | 75066030 | intron variant | A/G | snv | 0.34 | 1 | ||
rs11842874 | 1.000 | 0.040 | 13 | 113040195 | intron variant | A/G | snv | 0.12 | 1 |