Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs9350 | 0.742 | 0.240 | 1 | 241885372 | missense variant | C/T | snv | 0.21 | 0.19 | 16 | |
rs121434596 | 0.677 | 0.440 | 1 | 114716123 | missense variant | C/A;G;T | snv | 4.0E-06; 4.0E-06 | 14 | ||
rs121913250 | 0.683 | 0.440 | 1 | 114716127 | missense variant | C/A;G;T | snv | 14 | |||
rs1057519902 | 0.742 | 0.160 | 1 | 226064451 | missense variant | G/C | snv | 13 | |||
rs1553260624 | 0.763 | 0.080 | 1 | 226064454 | missense variant | G/A | snv | 13 | |||
rs2516839 | 0.732 | 0.320 | 1 | 161043331 | 5 prime UTR variant | C/T | snv | 0.49 | 13 | ||
rs397514606 | 0.763 | 0.320 | 1 | 243695714 | missense variant | C/T | snv | 13 | |||
rs12733285 | 0.776 | 0.120 | 1 | 202952912 | intron variant | C/T | snv | 0.26 | 12 | ||
rs1342387 | 0.776 | 0.120 | 1 | 202945228 | intron variant | T/C | snv | 0.53 | 12 | ||
rs172378 | 0.790 | 0.240 | 1 | 22638945 | synonymous variant | A/G | snv | 0.49 | 0.51 | 11 | |
rs4645981 | 0.790 | 0.160 | 1 | 15524988 | intron variant | G/A;C | snv | 11 | |||
rs627928 | 0.790 | 0.080 | 1 | 182582202 | missense variant | A/C | snv | 0.54 | 0.49 | 10 | |
rs796065343 | 0.776 | 0.080 | 1 | 36467833 | missense variant | G/A | snv | 10 | |||
rs11801299 | 0.807 | 0.200 | 1 | 204559956 | downstream gene variant | G/A | snv | 0.16 | 9 | ||
rs1012477 | 0.827 | 0.160 | 1 | 7798075 | intron variant | G/C | snv | 0.16 | 8 | ||
rs11249433 | 0.827 | 0.160 | 1 | 121538815 | intron variant | A/C;G | snv | 8 | |||
rs3021094 | 0.827 | 0.360 | 1 | 206771607 | intron variant | T/G | snv | 8.0E-02 | 8 | ||
rs121913255 | 0.667 | 0.400 | 1 | 114713907 | missense variant | T/A;G | snv | 7 | |||
rs3790843 | 0.827 | 0.160 | 1 | 200041696 | intron variant | C/T | snv | 0.29 | 7 | ||
rs769809364 | 0.807 | 0.080 | 1 | 3732940 | missense variant | G/A | snv | 8.5E-06 | 1.4E-05 | 7 | |
rs1332018 | 0.882 | 0.200 | 1 | 109740350 | 5 prime UTR variant | G/T | snv | 0.64 | 0.66 | 6 | |
rs5273 | 0.827 | 0.080 | 1 | 186674636 | missense variant | A/C;G | snv | 4.0E-06; 7.6E-03 | 1.4E-02 | 6 | |
rs121434264 | 0.851 | 0.080 | 1 | 193125171 | missense variant | T/C | snv | 5 | |||
rs3126085 | 0.851 | 0.280 | 1 | 152328341 | intron variant | G/A | snv | 0.29 | 5 | ||
rs35301225 | 0.882 | 0.080 | 1 | 9151743 | mature miRNA variant | C/A;T | snv | 5 |