Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs802791 | 0.851 | 0.160 | 6 | 106121395 | intron variant | T/C | snv | 0.75 | 4 | ||
rs906868 | 0.925 | 0.120 | 2 | 30225478 | intergenic variant | G/T | snv | 0.53 | 4 | ||
rs911263 | 0.851 | 0.200 | 14 | 68286876 | intron variant | C/T | snv | 0.57 | 4 | ||
rs9268832 | 0.882 | 0.160 | 6 | 32460012 | non coding transcript exon variant | T/C | snv | 0.61 | 0.59 | 4 | |
rs9275328 | 0.851 | 0.240 | 6 | 32699045 | intergenic variant | C/T | snv | 0.16 | 4 | ||
rs1051792 | 0.851 | 0.240 | 6 | 31411200 | missense variant | G/A | snv | 0.34 | 0.35 | 5 | |
rs12531711 | 0.827 | 0.200 | 7 | 128977412 | intron variant | A/C;G | snv | 5 | |||
rs12537 | 0.827 | 0.280 | 22 | 30027471 | 3 prime UTR variant | C/T | snv | 0.40 | 5 | ||
rs13238352 | 0.827 | 0.240 | 7 | 129007888 | intron variant | C/T | snv | 9.1E-02 | 5 | ||
rs17849502 | 0.827 | 0.240 | 1 | 183563445 | missense variant | G/A;C;T | snv | 4.0E-06; 4.0E-06; 3.4E-02 | 5 | ||
rs2239804 | 0.851 | 0.240 | 6 | 32443746 | intron variant | T/A;C | snv | 0.51 | 5 | ||
rs2251396 | 0.827 | 0.240 | 6 | 31396930 | upstream gene variant | G/A | snv | 0.24 | 5 | ||
rs2395174 | 0.827 | 0.320 | 6 | 32437101 | upstream gene variant | T/G | snv | 0.24 | 5 | ||
rs2431098 | 0.827 | 0.240 | 5 | 160460329 | intron variant | A/G;T | snv | 5 | |||
rs2736337 | 0.827 | 0.240 | 8 | 11484371 | upstream gene variant | T/C | snv | 0.26 | 5 | ||
rs2858331 | 0.827 | 0.240 | 6 | 32713500 | upstream gene variant | A/G | snv | 0.42 | 5 | ||
rs2900180 | 0.827 | 0.280 | 9 | 120944104 | regulatory region variant | T/A;C | snv | 5 | |||
rs3129890 | 0.827 | 0.280 | 6 | 32446496 | downstream gene variant | T/A;C | snv | 5 | |||
rs3129939 | 0.827 | 0.360 | 6 | 32368989 | intron variant | A/G | snv | 0.14 | 5 | ||
rs3130320 | 0.851 | 0.160 | 6 | 32255481 | intron variant | T/C | snv | 0.68 | 5 | ||
rs3130340 | 0.851 | 0.200 | 6 | 32276850 | intron variant | T/C | snv | 0.25 | 5 | ||
rs35929052 | 0.827 | 0.160 | 16 | 85960878 | downstream gene variant | C/G;T | snv | 5 | |||
rs4085613 | 0.827 | 0.160 | 1 | 152577542 | downstream gene variant | T/G | snv | 0.59 | 5 | ||
rs560051377 | 0.851 | 0.320 | 1 | 161624624 | missense variant | G/A;C | snv | 4.0E-06; 2.8E-05 | 5 | ||
rs6659932 | 0.827 | 0.240 | 1 | 67336688 | intron variant | A/C | snv | 0.81 | 5 |