Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs212389 | 0.925 | 0.160 | 6 | 159068759 | non coding transcript exon variant | G/A | snv | 0.60 | 3 | ||
rs4648356 | 1.000 | 0.080 | 1 | 2792599 | intron variant | C/A | snv | 0.39 | 3 | ||
rs11586238 | 0.925 | 0.160 | 1 | 116720516 | regulatory region variant | C/G | snv | 0.19 | 4 | ||
rs11676922 | 0.925 | 0.160 | 2 | 100190478 | intron variant | T/A | snv | 0.51 | 4 | ||
rs13315591 | 0.925 | 0.160 | 3 | 58571114 | intron variant | T/C | snv | 0.15 | 4 | ||
rs26232 | 0.925 | 0.160 | 5 | 103261019 | intron variant | C/T | snv | 0.30 | 4 | ||
rs3093023 | 0.851 | 0.160 | 6 | 167120802 | intron variant | G/A | snv | 0.34 | 4 | ||
rs3761847 | 0.827 | 0.200 | 9 | 120927961 | intron variant | G/A | snv | 0.52 | 4 | ||
rs4750316 | 0.882 | 0.160 | 10 | 6351298 | non coding transcript exon variant | C/G;T | snv | 4 | |||
rs4810485 | 0.732 | 0.480 | 20 | 46119308 | intron variant | T/A;G | snv | 4 | |||
rs548234 | 0.763 | 0.360 | 6 | 106120159 | intron variant | C/T | snv | 0.76 | 4 | ||
rs6859219 | 0.925 | 0.160 | 5 | 56142753 | intron variant | C/A | snv | 0.20 | 4 | ||
rs706778 | 0.695 | 0.320 | 10 | 6056986 | intron variant | C/T | snv | 0.46 | 4 | ||
rs743777 | 0.827 | 0.200 | 22 | 37155567 | intron variant | A/G | snv | 0.36 | 4 | ||
rs874040 | 0.925 | 0.160 | 4 | 26106575 | downstream gene variant | G/C | snv | 0.29 | 4 | ||
rs934734 | 0.925 | 0.160 | 2 | 65368452 | intron variant | G/A;T | snv | 0.54 | 4 | ||
rs951005 | 0.807 | 0.200 | 9 | 34743684 | intron variant | G/A | snv | 0.78 | 4 | ||
rs10806425 | 0.851 | 0.280 | 6 | 90216893 | intron variant | C/A | snv | 0.33 | 5 | ||
rs10903122 | 0.882 | 0.200 | 1 | 24977085 | intergenic variant | A/G | snv | 0.56 | 5 | ||
rs11221332 | 0.763 | 0.280 | 11 | 128511079 | intron variant | C/A;T | snv | 5 | |||
rs11712165 | 0.882 | 0.200 | 3 | 119399949 | intron variant | T/G | snv | 0.30 | 5 | ||
rs1250552 | 0.882 | 0.200 | 10 | 79298270 | intron variant | A/C;G | snv | 5 | |||
rs12928822 | 0.882 | 0.200 | 16 | 11310036 | intron variant | C/T | snv | 0.13 | 5 | ||
rs13010713 | 0.882 | 0.200 | 2 | 181131318 | intron variant | A/C;G | snv | 5 | |||
rs13098911 | 0.882 | 0.200 | 3 | 46193709 | intron variant | C/G;T | snv | 5 |