Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs179363875 | 0.882 | 0.080 | 21 | 44286049 | missense variant | C/T | snv | 3 | |||
rs1437439236 | 0.925 | 0.080 | 10 | 70871945 | missense variant | C/T | snv | 8.0E-06 | 3 | ||
rs12917716 | 0.851 | 0.200 | 16 | 11095291 | intron variant | G/C | snv | 0.51 | 4 | ||
rs8048002 | 0.851 | 0.320 | 16 | 10898131 | intron variant | T/A;C | snv | 4 | |||
rs6161 | 0.851 | 0.080 | 15 | 74343027 | missense variant | C/T | snv | 2.5E-03 | 2.6E-03 | 5 | |
rs6498169 | 0.807 | 0.280 | 16 | 11155472 | non coding transcript exon variant | G/A | snv | 0.66 | 6 | ||
rs121918654 | 0.882 | 0.200 | 9 | 124503218 | missense variant | GC/TT | mnv | 6 | |||
rs12708716 | 0.807 | 0.320 | 16 | 11086016 | intron variant | A/G | snv | 0.37 | 7 | ||
rs763361 | 0.689 | 0.520 | 18 | 69864406 | missense variant | T/A;C | snv | 4.0E-06; 0.52 | 21 | ||
rs237025 | 0.672 | 0.360 | 6 | 149400554 | missense variant | G/A | snv | 0.55 | 0.57 | 26 | |
rs1990760 | 0.672 | 0.480 | 2 | 162267541 | missense variant | C/T | snv | 0.50 | 0.45 | 33 | |
rs56149945 | 0.595 | 0.680 | 5 | 143399752 | missense variant | T/A;C | snv | 2.0E-02 | 49 | ||
rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 121 |