Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 14 | |
rs671 | 0.529 | 0.840 | 12 | 111803962 | missense variant | G/A | snv | 1.9E-02 | 5.8E-03 | 10 | |
rs10069690 | 0.595 | 0.560 | 5 | 1279675 | intron variant | C/T | snv | 0.36 | 4 | ||
rs10505477 | 0.658 | 0.400 | 8 | 127395198 | intron variant | A/G | snv | 0.40 | 3 | ||
rs1801133 | 0.472 | 0.880 | 1 | 11796321 | missense variant | G/A | snv | 0.31 | 0.27 | 3 | |
rs3803662 | 0.662 | 0.440 | 16 | 52552429 | non coding transcript exon variant | A/G | snv | 0.63 | 3 | ||
rs3814113 | 0.827 | 0.200 | 9 | 16915023 | upstream gene variant | T/C | snv | 0.41 | 3 | ||
rs6983267 | 0.578 | 0.440 | 8 | 127401060 | non coding transcript exon variant | G/T | snv | 0.37 | 3 | ||
rs8170 | 0.724 | 0.160 | 19 | 17278895 | synonymous variant | G/A | snv | 0.15 | 0.18 | 3 | |
rs11571833 | 0.608 | 0.360 | 13 | 32398489 | stop gained | A/T | snv | 6.6E-03 | 6.0E-03 | 2 | |
rs11651755 | 0.763 | 0.160 | 17 | 37739849 | intron variant | T/C | snv | 0.52 | 2 | ||
rs13281615 | 0.716 | 0.360 | 8 | 127343372 | intron variant | A/G | snv | 0.43 | 2 | ||
rs17251221 | 0.724 | 0.360 | 3 | 122274400 | intron variant | A/G | snv | 0.11 | 2 | ||
rs2153271 | 0.925 | 0.160 | 9 | 16864523 | intron variant | C/T | snv | 0.43 | 2 | ||
rs2363956 | 0.776 | 0.160 | 19 | 17283315 | missense variant | T/G | snv | 0.48 | 0.50 | 2 | |
rs2660753 | 0.790 | 0.240 | 3 | 87061524 | intergenic variant | T/C | snv | 0.76 | 2 | ||
rs2981582 | 0.695 | 0.360 | 10 | 121592803 | intron variant | A/G | snv | 0.58 | 2 | ||
rs10088218 | 0.851 | 0.120 | 8 | 128531703 | intron variant | G/A | snv | 0.13 | 1 | ||
rs10756819 | 1.000 | 0.120 | 9 | 16858086 | intron variant | G/A;C;T | snv | 1 | |||
rs10810666 | 1.000 | 0.120 | 9 | 16911668 | intergenic variant | C/T | snv | 0.14 | 1 | ||
rs10962656 | 1.000 | 0.120 | 9 | 16877790 | intergenic variant | G/A | snv | 0.10 | 1 | ||
rs11782652 | 0.851 | 0.120 | 8 | 81741409 | intron variant | A/G | snv | 6.6E-02 | 1 | ||
rs12373237 | 0.851 | 0.200 | 18 | 23845972 | intron variant | G/A | snv | 0.47 | 1 | ||
rs12379183 | 1.000 | 0.120 | 9 | 16865701 | intron variant | A/G | snv | 0.26 | 1 | ||
rs12379687 | 1.000 | 0.120 | 9 | 16854369 | intron variant | G/A;T | snv | 1 |