Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs763802417 | 0.882 | 0.040 | X | 100862805 | missense variant | G/A | snv | 5.9E-06 | 5 | ||
rs5031002 | 1.000 | 0.040 | X | 67722783 | intron variant | G/A | snv | 1.5E-02 | 1.5E-02 | 3 | |
rs16999497 | 0.925 | 0.040 | X | 129601222 | regulatory region variant | T/C | snv | 7.8E-02 | 2 | ||
rs5943057 | 1.000 | 0.040 | X | 110695977 | intron variant | T/G | snv | 0.50 | 1 | ||
rs755622 | 0.611 | 0.720 | 22 | 23894205 | intron variant | G/C | snv | 0.26 | 44 | ||
rs1232898090 | 0.637 | 0.600 | 22 | 46198429 | missense variant | G/C;T | snv | 4.0E-06; 4.0E-06 | 40 | ||
rs1800206 | 0.641 | 0.640 | 22 | 46218377 | missense variant | C/G | snv | 4.3E-02 | 4.2E-02 | 35 | |
rs4818 | 0.683 | 0.440 | 22 | 19963684 | synonymous variant | C/G;T | snv | 0.34 | 27 | ||
rs1065852 | 0.695 | 0.360 | 22 | 42130692 | missense variant | G/A | snv | 0.21 | 0.19 | 19 | |
rs1465444723 | 0.827 | 0.240 | 22 | 30610886 | missense variant | A/G | snv | 4.0E-06 | 5 | ||
rs133049 | 0.882 | 0.080 | 22 | 40635351 | intron variant | A/- | delins | 0.82 | 4 | ||
rs7291467 | 0.851 | 0.160 | 22 | 37576621 | intron variant | G/A | snv | 0.49 | 4 | ||
rs12165908 | 1.000 | 0.040 | 22 | 19777658 | intron variant | G/C | snv | 0.20 | 1 | ||
rs75680863 | 1.000 | 0.040 | 22 | 30611036 | missense variant | A/G;T | snv | 2.7E-03 | 1 | ||
rs1051266 | 0.627 | 0.640 | 21 | 45537880 | missense variant | T/C;G | snv | 0.55; 4.4E-06 | 41 | ||
rs777919630 | 0.623 | 0.680 | 21 | 43062358 | missense variant | G/A;T | snv | 8.0E-06; 4.0E-06 | 40 | ||
rs1202989817 | 0.716 | 0.360 | 21 | 31659813 | missense variant | T/C;G | snv | 8.0E-06 | 7.0E-06 | 18 | |
rs460976 | 0.851 | 0.120 | 21 | 41463567 | downstream gene variant | A/G;T | snv | 7 | |||
rs121964962 | 0.827 | 0.200 | 21 | 43062988 | missense variant | C/T | snv | 1.6E-04 | 5 | ||
rs9982601 | 0.851 | 0.080 | 21 | 34226827 | intron variant | C/T | snv | 0.15 | 4 | ||
rs2254638 | 0.882 | 0.040 | 21 | 28883961 | intron variant | A/C;G | snv | 3 | |||
rs428785 | 0.882 | 0.040 | 21 | 26844276 | missense variant | C/A;G;T | snv | 1.3E-05; 0.70 | 0.78 | 3 | |
rs771748290 | 0.882 | 0.160 | 21 | 43072114 | missense variant | C/A;T | snv | 8.1E-06; 8.1E-06 | 3 | ||
rs779011920 | 0.882 | 0.160 | 21 | 43066299 | missense variant | C/T | snv | 8.0E-06 | 3 | ||
rs143081213 | 1.000 | 0.040 | 21 | 34615168 | upstream gene variant | G/A | snv | 2.6E-02 | 2 |