Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs478442 | 0.851 | 0.120 | 2 | 21176344 | intergenic variant | G/C;T | snv | 18 | |||
rs4803750 | 0.807 | 0.240 | 19 | 44744370 | upstream gene variant | A/G | snv | 7.7E-02 | 22 | ||
rs4905014 | 0.851 | 0.120 | 14 | 92945686 | intron variant | G/A;C | snv | 16 | |||
rs5068 | 0.776 | 0.160 | 1 | 11845917 | 3 prime UTR variant | A/G;T | snv | 13 | |||
rs5418 | 1.000 | 0.040 | 17 | 7281773 | 5 prime UTR variant | G/A | snv | 0.49 | 3 | ||
rs562338 | 0.807 | 0.160 | 2 | 21065449 | intergenic variant | A/G | snv | 0.69 | 21 | ||
rs5744680 | 0.851 | 0.120 | 5 | 75584065 | intron variant | G/A | snv | 0.55 | 18 | ||
rs629301 | 0.851 | 0.120 | 1 | 109275684 | 3 prime UTR variant | G/T | snv | 0.74 | 22 | ||
rs6533530 | 0.851 | 0.120 | 4 | 110810780 | intergenic variant | T/C | snv | 0.47 | 16 | ||
rs6759518 | 0.851 | 0.120 | 2 | 27263727 | intron variant | G/C | snv | 5.5E-02 | 16 | ||
rs7115242 | 0.851 | 0.120 | 11 | 117037567 | intron variant | A/G;T | snv | 16 | |||
rs7190256 | 0.851 | 0.120 | 16 | 72963084 | intron variant | C/T | snv | 0.94 | 16 | ||
rs760762 | 0.851 | 0.120 | 20 | 41147406 | intron variant | C/A;T | snv | 0.59 | 16 | ||
rs7632505 | 0.827 | 0.120 | 3 | 123019460 | intron variant | A/G | snv | 0.34 | 17 | ||
rs765547 | 0.827 | 0.160 | 8 | 20008763 | intergenic variant | G/A;C;T | snv | 18 | |||
rs7703051 | 0.851 | 0.120 | 5 | 75329662 | intron variant | C/A | snv | 0.38 | 18 | ||
rs780094 | 0.658 | 0.400 | 2 | 27518370 | intron variant | T/C | snv | 0.67 | 62 | ||
rs7903146 | 0.554 | 0.680 | 10 | 112998590 | intron variant | C/G;T | snv | 93 | |||
rs799165 | 0.851 | 0.120 | 7 | 73637727 | intergenic variant | T/A | snv | 0.13 | 17 | ||
rs8082812 | 0.851 | 0.120 | 18 | 8522684 | intergenic variant | C/A | snv | 4.6E-02 | 16 | ||
rs964184 | 0.716 | 0.440 | 11 | 116778201 | 3 prime UTR variant | G/C | snv | 0.82 | 47 | ||
rs9939609 | 0.559 | 0.720 | 16 | 53786615 | intron variant | T/A | snv | 0.41 | 98 | ||
rs1799945 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 226 | |
rs1047891 | 0.827 | 0.200 | 2 | 210675783 | missense variant | C/A | snv | 0.30 | 0.33 | 34 | |
rs699 | 0.501 | 0.800 | 1 | 230710048 | missense variant | A/G | snv | 0.55 | 0.58 | 134 |