Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs603424 | 1.000 | 0.080 | 10 | 100315722 | intron variant | G/A | snv | 0.34 | 13 | ||
rs13114738 | 0.851 | 0.120 | 4 | 102363708 | intron variant | C/A;T | snv | 16 | |||
rs629301 | 0.851 | 0.120 | 1 | 109275684 | 3 prime UTR variant | G/T | snv | 0.74 | 22 | ||
rs2087160 | 4 | 110413574 | intron variant | G/T | snv | 0.68 | 2 | ||||
rs9393903 | 6 | 11042676 | intron variant | G/A | snv | 0.18 | 3 | ||||
rs6533530 | 0.851 | 0.120 | 4 | 110810780 | intergenic variant | T/C | snv | 0.47 | 16 | ||
rs79105258 | 12 | 111280427 | intron variant | C/A;T | snv | 24 | |||||
rs7760535 | 6 | 111425880 | intron variant | G/C | snv | 0.46 | 3 | ||||
rs4506565 | 0.790 | 0.280 | 10 | 112996282 | intron variant | A/G;T | snv | 22 | |||
rs7903146 | 0.554 | 0.680 | 10 | 112998590 | intron variant | C/G;T | snv | 93 | |||
rs10885409 | 1.000 | 0.080 | 10 | 113048313 | intron variant | T/C | snv | 0.54 | 3 | ||
rs964184 | 0.716 | 0.440 | 11 | 116778201 | 3 prime UTR variant | G/C | snv | 0.82 | 47 | ||
rs7115242 | 0.851 | 0.120 | 11 | 117037567 | intron variant | A/G;T | snv | 16 | |||
rs13266634 | 0.724 | 0.480 | 8 | 117172544 | missense variant | C/A;T | snv | 0.29 | 23 | ||
rs477992 | 1 | 119714953 | intron variant | A/G | snv | 0.69 | 4 | ||||
rs9943291 | 1 | 119749667 | intron variant | T/G | snv | 8.2E-02 | 3 | ||||
rs2066938 | 12 | 120722812 | 3 prime UTR variant | A/C;G | snv | 3 | |||||
rs2650000 | 0.851 | 0.200 | 12 | 120951159 | intron variant | A/C | snv | 0.70 | 10 | ||
rs12369179 | 0.851 | 0.120 | 12 | 122479003 | intron variant | C/T | snv | 5.9E-02 | 16 | ||
rs12420422 | 0.851 | 0.120 | 11 | 123009573 | intergenic variant | G/A | snv | 3.4E-02 | 16 | ||
rs7632505 | 0.827 | 0.120 | 3 | 123019460 | intron variant | A/G | snv | 0.34 | 17 | ||
rs2980853 | 0.851 | 0.120 | 8 | 125466108 | upstream gene variant | A/C | snv | 0.43 | 16 | ||
rs272889 | 5 | 132329685 | intron variant | A/G | snv | 0.64 | 2 | ||||
rs612169 | 9 | 133268030 | intron variant | G/A | snv | 10 | |||||
rs1869717 | 0.851 | 0.120 | 4 | 139829967 | intron variant | G/C | snv | 0.14 | 16 |