Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs5742626 | 12 | 102464131 | intron variant | T/C | snv | 2.3E-02 | 3 | ||||
rs5742692 | 12 | 102405820 | intron variant | A/G | snv | 6.6E-02 | 2 | ||||
rs5742617 | 12 | 102476127 | intron variant | C/T | snv | 8.7E-03 | 1 | ||||
rs5742643 | 12 | 102444085 | intron variant | T/C | snv | 0.76 | 1 | ||||
rs5742663 | 12 | 102430212 | intron variant | T/A;G | snv | 1 | |||||
rs5742683 | 12 | 102419939 | intron variant | A/G | snv | 3.3E-02 | 1 | ||||
rs7300373 | 12 | 102438008 | intron variant | T/G | snv | 1.4E-02 | 1 | ||||
rs9308315 | 12 | 102410115 | intron variant | A/C;T | snv | 1 | |||||
rs6214 | 0.672 | 0.400 | 12 | 102399791 | 3 prime UTR variant | C/T | snv | 0.45 | 26 | ||
rs6218 | 0.732 | 0.440 | 12 | 102399855 | 3 prime UTR variant | A/G | snv | 2.1E-02 | 13 | ||
rs5742612 | 0.752 | 0.440 | 12 | 102481086 | intron variant | A/G | snv | 5.6E-02 | 11 | ||
rs35767 | 0.763 | 0.360 | 12 | 102481791 | upstream gene variant | A/C;G;T | snv | 13 | |||
rs745805222 | 0.790 | 0.120 | 12 | 102475722 | synonymous variant | C/T | snv | 1.2E-05 | 4.9E-05 | 7 | |
rs972936 | 0.807 | 0.200 | 12 | 102431143 | intron variant | T/C | snv | 0.70 | 12 | ||
rs1520220 | 0.807 | 0.280 | 12 | 102402744 | intron variant | G/C;T | snv | 0.76 | 9 | ||
rs2195239 | 0.851 | 0.240 | 12 | 102462924 | non coding transcript exon variant | C/G | snv | 0.28 | 7 | ||
rs2162679 | 0.851 | 0.240 | 12 | 102477481 | intron variant | C/G;T | snv | 6 | |||
rs5742632 | 0.851 | 0.120 | 12 | 102462696 | intron variant | A/G | snv | 0.26 | 4 | ||
rs7136446 | 0.882 | 0.160 | 12 | 102444737 | intron variant | C/T | snv | 0.66 | 8 | ||
rs5742714 | 0.882 | 0.160 | 12 | 102396074 | 3 prime UTR variant | C/G | snv | 8.9E-02 | 3 | ||
rs12423791 | 0.925 | 0.040 | 12 | 102465050 | intron variant | G/C | snv | 2.8E-02 | 5 | ||
rs6220 | 0.925 | 0.080 | 12 | 102400737 | 3 prime UTR variant | G/A | snv | 0.67 | 4 | ||
rs1239905891 | 0.925 | 0.080 | 12 | 102475786 | missense variant | G/A;T | snv | 3 | |||
rs2072592 | 0.925 | 0.120 | 12 | 102419854 | intron variant | C/T | snv | 2.8E-02 | 2 | ||
rs2288377 | 0.925 | 0.080 | 12 | 102480984 | intron variant | A/G;T | snv | 2 |