Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1695 | 0.457 | 0.880 | 11 | 67585218 | missense variant | A/G | snv | 0.34 | 0.36 | 187 | |
rs121912664 | 0.630 | 0.320 | 17 | 7670699 | missense variant | C/A;G;T | snv | 1.2E-05 | 40 | ||
rs568887534 | 0.807 | 0.240 | 8 | 30183156 | missense variant | A/G | snv | 4.0E-06 | 9 | ||
rs1250394819 | 0.807 | 0.240 | 5 | 115616325 | missense variant | C/T | snv | 4.0E-06 | 9 | ||
rs1190999960 | 0.807 | 0.240 | 11 | 65571690 | missense variant | G/A | snv | 9 | |||
rs148634289 | 0.827 | 0.200 | 11 | 112088925 | synonymous variant | C/T | snv | 1.6E-05 | 2.1E-05 | 6 | |
rs1285675735 | 0.827 | 0.200 | 15 | 45043384 | synonymous variant | C/G;T | snv | 1.1E-05; 1.1E-05 | 6 | ||
rs587780072 | 0.882 | 0.240 | 17 | 7674927 | missense variant | G/A;C | snv | 2.8E-05 | 3 | ||
rs11893842 | 0.925 | 0.160 | 2 | 219572251 | intron variant | A/G | snv | 0.45 | 2 | ||
rs1464311 | 1.000 | 0.080 | 3 | 118482382 | intron variant | T/C | snv | 0.12 | 1 | ||
rs587777706 | 1.000 | 0.080 | 10 | 42820527 | missense variant | G/A | snv | 1.6E-05 | 1.4E-05 | 1 |