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 | |
rs646776 | 0.752 | 0.240 | 1 | 109275908 | downstream gene variant | C/T | snv | 0.74 | 10 | ||
rs1799945 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 10 | |
rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 8 | ||
rs1229984 | 0.570 | 0.560 | 4 | 99318162 | missense variant | T/C;G | snv | 0.90 | 6 | ||
rs12413409 | 0.790 | 0.200 | 10 | 102959339 | intron variant | G/A | snv | 9.0E-02 | 6 | ||
rs660895 | 0.752 | 0.360 | 6 | 32609603 | intergenic variant | A/G | snv | 0.19 | 6 | ||
rs3129882 | 0.807 | 0.240 | 6 | 32441753 | intron variant | G/A | snv | 0.56 | 5 | ||
rs393152 | 0.851 | 0.160 | 17 | 45641777 | non coding transcript exon variant | A/G | snv | 0.18 | 0.29 | 5 | |
rs1864325 | 0.882 | 0.160 | 17 | 45900461 | intron variant | C/T | snv | 0.14 | 5 | ||
rs8070723 | 0.851 | 0.240 | 17 | 46003698 | intron variant | A/G | snv | 0.18 | 5 | ||
rs2070600 | 0.561 | 0.760 | 6 | 32183666 | missense variant | C/T | snv | 5.3E-02 | 3.6E-02 | 4 | |
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 4 | |
rs546433642 | 0.925 | 0.120 | 17 | 46172742 | intron variant | T/C;G | snv | 4 | |||
rs549599956 | 0.925 | 0.120 | 17 | 46169798 | intron variant | A/G | snv | 4 | |||
rs17651549 | 0.882 | 0.160 | 17 | 45983912 | missense variant | C/T | snv | 0.15 | 0.14 | 4 | |
rs17690703 | 0.882 | 0.160 | 17 | 45847931 | intron variant | C/T | snv | 0.18 | 4 | ||
rs12373139 | 0.925 | 0.120 | 17 | 45846764 | missense variant | G/A | snv | 0.15 | 0.14 | 4 | |
rs1805007 | 0.695 | 0.280 | 16 | 89919709 | missense variant | C/A;G;T | snv | 4.4E-02 | 4 | ||
rs199533 | 0.925 | 0.120 | 17 | 46751565 | synonymous variant | G/A | snv | 0.13 | 0.13 | 4 | |
rs12185233 | 0.882 | 0.160 | 17 | 45846288 | missense variant | G/A;C | snv | 9.5E-05; 0.15 | 4 | ||
rs12373123 | 0.882 | 0.160 | 17 | 45846707 | missense variant | T/C | snv | 0.15 | 0.14 | 4 | |
rs12373142 | 0.851 | 0.200 | 17 | 45846834 | missense variant | C/G;T | snv | 0.15 | 4 | ||
rs2395163 | 0.882 | 0.160 | 6 | 32420032 | intergenic variant | T/C | snv | 0.17 | 3 |