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 | |||
rs222826 | 0.851 | 0.120 | 2 | 146120964 | regulatory region variant | T/C | snv | 0.94 | 16 | ||
rs6759518 | 0.851 | 0.120 | 2 | 27263727 | intron variant | G/C | snv | 5.5E-02 | 16 | ||
rs16867253 | 0.851 | 0.120 | 2 | 9956965 | intron variant | G/T | snv | 5.8E-02 | 7 | ||
rs10189761 | 0.882 | 0.120 | 2 | 646364 | intergenic variant | T/A | snv | 0.82 | 4 | ||
rs267607499 | 0.851 | 0.160 | 2 | 219418809 | missense variant | A/G;T | snv | 4 | |||
rs10932374 | 0.925 | 0.040 | 2 | 211379678 | 3 prime UTR variant | G/A | snv | 0.23 | 2 | ||
rs13003941 | 0.925 | 0.040 | 2 | 211378978 | 3 prime UTR variant | G/C;T | snv | 0.26 | 2 | ||
rs1595064 | 0.925 | 0.040 | 2 | 211378020 | 3 prime UTR variant | G/A;C | snv | 2 | |||
rs1595065 | 0.925 | 0.040 | 2 | 211377916 | 3 prime UTR variant | G/A | snv | 0.73 | 2 | ||
rs3748960 | 0.925 | 0.040 | 2 | 211383109 | 3 prime UTR variant | C/T | snv | 0.96 | 2 | ||
rs1801282 | 0.500 | 0.840 | 3 | 12351626 | missense variant | C/G | snv | 0.11 | 8.9E-02 | 131 | |
rs1805192 | 0.510 | 0.840 | 3 | 12379739 | missense variant | C/G | snv | 121 | |||
rs5186 | 0.630 | 0.560 | 3 | 148742201 | 3 prime UTR variant | A/C | snv | 0.23 | 0.21 | 38 | |
rs7632505 | 0.827 | 0.120 | 3 | 123019460 | intron variant | A/G | snv | 0.34 | 17 | ||
rs7626962 | 0.790 | 0.080 | 3 | 38579416 | missense variant | G/A;T | snv | 1.6E-05; 5.9E-03 | 10 | ||
rs9838915 | 0.882 | 0.120 | 3 | 126347377 | intron variant | G/A | snv | 0.19 | 4 | ||
rs189919070 | 1.000 | 0.040 | 3 | 134436825 | upstream gene variant | C/A;T | snv | 3 | |||
rs1805126 | 0.925 | 0.040 | 3 | 38550915 | synonymous variant | A/G | snv | 0.39 | 0.44 | 2 | |
rs6787362 | 0.925 | 0.040 | 3 | 69178228 | intron variant | A/G | snv | 9.3E-02 | 2 | ||
rs12638540 | 1.000 | 0.040 | 3 | 32447042 | intron variant | A/G;T | snv | 1 | |||
rs28362491 | 0.592 | 0.720 | 4 | 102500998 | non coding transcript exon variant | ATTG/- | delins | 56 | |||
rs1799895 | 0.683 | 0.360 | 4 | 24800212 | missense variant | C/G | snv | 2.3E-02 | 1.2E-02 | 26 | |
rs1022113606 | 0.732 | 0.280 | 4 | 24800161 | missense variant | G/C | snv | 1.6E-04 | 2.1E-05 | 17 | |
rs13114738 | 0.851 | 0.120 | 4 | 102363708 | intron variant | C/A;T | snv | 16 |