Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7775698 | 1.000 | 0.080 | 6 | 135097497 | intron variant | C/T | snv | 6.9E-02 | 14 | ||
rs385893 | 0.925 | 0.080 | 9 | 4763176 | downstream gene variant | T/C | snv | 0.44 | 9 | ||
rs1265115 | 0.925 | 0.080 | 6 | 31149298 | non coding transcript exon variant | C/A;T | snv | 5 | |||
rs3130779 | 0.925 | 0.080 | 6 | 30904426 | upstream gene variant | A/C;G;T | snv | 5 | |||
rs3131034 | 0.925 | 0.080 | 6 | 30886019 | intron variant | G/A | snv | 0.75 | 5 | ||
rs4148876 | 0.925 | 0.080 | 6 | 32829016 | missense variant | G/A | snv | 7.6E-02 | 5.7E-02 | 4 | |
rs5745568 | 0.882 | 0.080 | 6 | 33580617 | intron variant | G/T | snv | 0.19 | 4 | ||
rs6141 | 0.925 | 0.080 | 3 | 184372478 | 3 prime UTR variant | C/G;T | snv | 4.0E-06; 0.56 | 4 | ||
rs2243873 | 1.000 | 0.080 | 6 | 31895656 | non coding transcript exon variant | C/A | snv | 0.61 | 3 | ||
rs3917267 | 0.882 | 0.080 | 2 | 102162359 | intron variant | G/A | snv | 0.32 | 3 | ||
rs7549785 | 0.925 | 0.080 | 1 | 159308078 | 3 prime UTR variant | G/A | snv | 0.13 | 3 | ||
rs12354 | 0.925 | 0.080 | 12 | 6390939 | 3 prime UTR variant | T/A;G | snv | 1.6E-04; 0.76 | 2 | ||
rs1866139 | 1.000 | 0.080 | 2 | 85694266 | intron variant | G/C | snv | 0.51 | 2 | ||
rs201339654 | 0.925 | 0.080 | 14 | 69786192 | missense variant | C/G;T | snv | 8.0E-06; 2.0E-05 | 2 | ||
rs2256609 | 0.925 | 0.080 | 22 | 21570728 | intron variant | A/G | snv | 0.18 | 2 | ||
rs2723175 | 1.000 | 0.080 | 2 | 112910176 | upstream gene variant | G/A | snv | 0.11 | 2 | ||
rs2856726 | 1.000 | 0.080 | 6 | 32698944 | intergenic variant | A/T | snv | 0.34 | 2 | ||
rs2858312 | 1.000 | 0.080 | 6 | 32699453 | intergenic variant | G/C | snv | 0.32 | 2 | ||
rs3135021 | 0.925 | 0.080 | 6 | 33077781 | intron variant | G/A | snv | 0.32 | 2 | ||
rs370229832 | 0.925 | 0.080 | 11 | 46739293 | missense variant | T/C | snv | 3.2E-05 | 6.3E-05 | 2 | |
rs3806798 | 0.925 | 0.080 | 4 | 141636126 | upstream gene variant | T/A | snv | 8.7E-02 | 2 | ||
rs4148871 | 0.925 | 0.080 | 6 | 32835539 | intron variant | A/G | snv | 0.82 | 2 | ||
rs5751902 | 1.000 | 0.080 | 22 | 24600663 | intron variant | C/T | snv | 0.29 | 2 | ||
rs5754344 | 1.000 | 0.080 | 22 | 21609497 | intron variant | A/G | snv | 0.18 | 2 | ||
rs6472812 | 1.000 | 0.080 | 8 | 74004849 | missense variant | A/G | snv | 0.97 | 0.97 | 2 |