Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1207112399 | 0.925 | 0.080 | 6 | 151842614 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 3 | |
rs760503206 | 0.925 | 0.080 | 6 | 151807956 | missense variant | T/C | snv | 4.0E-06 | 2 | ||
rs767863538 | 0.925 | 0.080 | 6 | 151808207 | missense variant | C/G;T | snv | 5.6E-06; 5.6E-06 | 3 | ||
rs757200716 | 0.851 | 0.160 | 6 | 151842617 | missense variant | G/A | snv | 8.0E-06 | 5 | ||
rs2077647 | 0.732 | 0.320 | 6 | 151807942 | synonymous variant | T/A;C | snv | 8.1E-06; 0.46 | 16 | ||
rs747099645 | 0.882 | 0.120 | 6 | 152061061 | missense variant | C/T | snv | 1.6E-05 | 2.8E-05 | 3 | |
rs761843408 | 0.925 | 0.080 | 6 | 152125285 | synonymous variant | A/G | snv | 3.4E-05 | 2.8E-05 | 2 | |
rs200282497 | 0.925 | 0.080 | 6 | 151944239 | missense variant | G/C | snv | 3.6E-05 | 3.5E-05 | 4 | |
rs188957694 | 0.882 | 0.080 | 6 | 151944218 | missense variant | G/A;C | snv | 4.0E-05 | 4.9E-05 | 6 | |
rs201145204 | 0.925 | 0.080 | 6 | 151808318 | missense variant | C/T | snv | 2.4E-04 | 1.0E-03 | 2 | |
rs139960913 | 1.000 | 0.080 | 6 | 151807928 | missense variant | C/T | snv | 3.3E-03 | 3.1E-03 | 1 | |
rs200075329 | 0.925 | 0.080 | 6 | 151808264 | missense variant | T/C | snv | 4.4E-03 | 4.3E-03 | 4 | |
rs746432 | 0.851 | 0.120 | 6 | 151808173 | synonymous variant | G/A;C | snv | 6.6E-02 | 7.0E-02 | 4 | |
rs2273206 | 0.851 | 0.280 | 6 | 152061176 | intron variant | G/T | snv | 0.17 | 0.22 | 5 | |
rs2228480 | 0.724 | 0.360 | 6 | 152098960 | synonymous variant | G/A | snv | 0.19 | 0.18 | 16 | |
rs1801132 | 0.689 | 0.320 | 6 | 151944387 | synonymous variant | G/C | snv | 0.73 | 0.80 | 22 |