Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4372063 | 1.000 | 0.080 | 9 | 5003338 | intron variant | G/A;C | snv | 1 | |||
rs41316003 | 1.000 | 0.040 | 9 | 5126343 | missense variant | G/A;C | snv | 4.4E-03 | 1 | ||
rs375678155 | 1.000 | 9 | 5064922 | missense variant | G/A;C;T | snv | 1.7E-05; 1.7E-05; 4.2E-06 | 1 | |||
rs77375493 | 0.458 | 0.760 | 9 | 5073770 | missense variant | G/A;T | snv | 3.5E-04 | 181 | ||
rs368927897 | 0.790 | 0.240 | 9 | 5072541 | missense variant | G/A;T | snv | 2.8E-05; 6.4E-05 | 8 | ||
rs7857730 | 0.925 | 0.040 | 9 | 5084049 | intron variant | G/A;T | snv | 0.63 | 2 | ||
rs12342421 | 0.851 | 0.080 | 9 | 5065750 | intron variant | G/C | snv | 0.23 | 4 | ||
rs12349785 | 0.882 | 0.080 | 9 | 5076613 | intron variant | G/C | snv | 0.23 | 3 | ||
rs121912472 | 0.925 | 0.080 | 9 | 5073742 | missense variant | G/C | snv | 2 | |||
rs150221602 | 1.000 | 0.040 | 9 | 5081828 | missense variant | G/C | snv | 4.2E-04 | 5.4E-04 | 1 | |
rs12339666 | 0.925 | 0.080 | 9 | 5063296 | intron variant | G/T | snv | 0.34 | 2 | ||
rs759031245 | 1.000 | 0.040 | 9 | 5022025 | missense variant | G/T | snv | 5.2E-05 | 1 | ||
rs10815148 | 0.882 | 0.080 | 9 | 5057284 | intron variant | T/A | snv | 0.33 | 3 | ||
rs3808850 | 0.925 | 0.080 | 9 | 4983311 | upstream gene variant | T/A;C | snv | 2 | |||
rs12343867 | 0.790 | 0.200 | 9 | 5074189 | intron variant | T/C | snv | 0.25 | 9 | ||
rs182123615 | 0.807 | 0.200 | 9 | 5070058 | splice region variant | T/C | snv | 3.6E-04 | 1.1E-03 | 7 | |
rs4495487 | 0.925 | 0.080 | 9 | 5072798 | intron variant | T/C | snv | 0.23 | 3 | ||
rs1159782 | 1.000 | 0.040 | 9 | 5078117 | intron variant | T/C | snv | 0.23 | 1 | ||
rs923941004 | 1.000 | 0.040 | 9 | 5078334 | missense variant | T/C | snv | 1 | |||
rs764634461 | 1.000 | 0.080 | 9 | 5072516 | missense variant | T/G | snv | 1.2E-05 | 2.8E-05 | 1 |