Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121908987 | 0.742 | 0.200 | 7 | 151576412 | missense variant | C/A;G;T | snv | 4.0E-06 | 12 | ||
rs60682848 | 0.790 | 0.200 | 1 | 156134838 | stop gained | C/T | snv | 7.0E-06 | 11 | ||
rs120074192 | 0.763 | 0.120 | 11 | 2527959 | missense variant | A/G | snv | 10 | |||
rs3825214 | 0.851 | 0.080 | 12 | 114357638 | intron variant | G/A | snv | 0.77 | 8 | ||
rs121913003 | 0.882 | 0.200 | 2 | 219421532 | missense variant | C/T | snv | 6 | |||
rs267598596 | 0.827 | 0.120 | 1 | 40818164 | missense variant | G/A | snv | 5 | |||
rs57629361 | 0.827 | 0.280 | 1 | 156137207 | missense variant | C/A;G;T | snv | 9.3E-06 | 5 | ||
rs41310765 | 0.882 | 0.120 | 3 | 38575424 | missense variant | G/A | snv | 1.4E-04 | 7.7E-05 | 5 | |
rs199473039 | 0.851 | 0.120 | 7 | 150951512 | missense variant | G/A;C;T | snv | 9.5E-05 | 4 | ||
rs120074189 | 0.851 | 0.120 | 11 | 2778003 | missense variant | C/T | snv | 4 | |||
rs72549410 | 0.851 | 0.120 | 3 | 38606058 | missense variant | C/T | snv | 4 | |||
rs199472954 | 0.882 | 0.120 | 7 | 150951514 | missense variant | A/G;T | snv | 3 | |||
rs104894074 | 0.925 | 0.120 | 8 | 11708467 | missense variant | C/T | snv | 2 | |||
rs759067821 | 1.000 | 0.080 | 8 | 11758294 | missense variant | C/T | snv | 2.8E-05 | 1.4E-05 | 2 | |
rs758277832 | 1.000 | 0.080 | 5 | 173233109 | missense variant | G/C | snv | 2 | |||
rs172149856 | 0.925 | 0.080 | 19 | 49188641 | missense variant | G/A | snv | 5.1E-04 | 4.3E-04 | 2 | |
rs753734843 | 1.000 | 0.080 | 15 | 73322804 | missense variant | C/A;T | snv | 6.6E-06; 2.6E-05 | 1 |