Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1057520529 | 0.851 | 0.320 | X | 49251440 | missense variant | C/T | snv | 5 | |||
rs879253740 | 0.882 | 0.240 | 14 | 74493191 | splice donor variant | A/G | snv | 5 | |||
rs587782477 | 0.882 | 0.120 | 5 | 112775679 | missense variant | A/T | snv | 4 | |||
rs1217371203 | 0.882 | 0.120 | 3 | 122106342 | missense variant | A/G;T | snv | 4.0E-06; 4.0E-06 | 4 | ||
rs5743313 | 0.851 | 0.200 | 4 | 186079213 | intron variant | C/T | snv | 0.19 | 4 | ||
rs868435969 | 0.925 | 0.280 | 9 | 35066710 | missense variant | G/A | snv | 3 | |||
rs4308977 | 0.925 | 0.160 | 1 | 207473553 | missense variant | T/A;C | snv | 4.0E-06; 0.27 | 2 | ||
rs17616 | 1.000 | 0.080 | 1 | 207473578 | missense variant | G/A | snv | 0.26 | 0.30 | 1 |