Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 24 | ||
rs17145750 | 0.925 | 0.120 | 7 | 73612048 | intron variant | C/A;T | snv | 7 | |||
rs13022873 | 0.882 | 0.120 | 2 | 27592643 | intron variant | A/C;T | snv | 6 | |||
rs4666002 | 0.925 | 0.120 | 2 | 27617773 | intron variant | G/A;C | snv | 6 | |||
rs115810 | 0.925 | 0.120 | 6 | 25975655 | intron variant | G/A;C | snv | 5 | |||
rs11983997 | 0.925 | 0.120 | 7 | 73524914 | upstream gene variant | G/A;C | snv | 5 | |||
rs1540276 | 0.925 | 0.120 | 6 | 26028591 | upstream gene variant | T/A;G | snv | 5 | |||
rs199734 | 0.925 | 0.120 | 6 | 25940165 | intergenic variant | G/A;C | snv | 5 | |||
rs199737 | 0.925 | 0.120 | 6 | 25933310 | upstream gene variant | A/C;T | snv | 5 | |||
rs2794719 | 0.925 | 0.120 | 6 | 26088662 | intron variant | T/C;G | snv | 5 | |||
rs386406569 | 0.925 | 0.120 | 6 | 26101212 | upstream gene variant | -/C | delins | 5 | |||
rs4665987 | 0.925 | 0.120 | 2 | 27532958 | upstream gene variant | G/A;T | snv | 5 | |||
rs6760250 | 0.925 | 0.120 | 2 | 27589385 | intron variant | G/A;C | snv | 5 | |||
rs807212 | 0.925 | 0.120 | 6 | 26065393 | regulatory region variant | A/G;T | snv | 5 | |||
rs9379818 | 0.925 | 0.120 | 6 | 26022978 | downstream gene variant | G/A;T | snv | 5 | |||
rs10946785 | 0.925 | 0.120 | 6 | 25616840 | intron variant | G/A;T | snv | 4 | |||
rs1165151 | 0.925 | 0.120 | 6 | 25821388 | intron variant | T/A;G | snv | 4 | |||
rs1165152 | 0.925 | 0.120 | 6 | 25818538 | intron variant | A/C;G;T | snv | 4 | |||
rs1165153 | 0.925 | 0.120 | 6 | 25817561 | intron variant | A/G;T | snv | 4 | |||
rs1165205 | 0.925 | 0.120 | 6 | 25870314 | intron variant | T/A;G | snv | 4 | |||
rs1184804 | 0.925 | 0.120 | 6 | 25867998 | intron variant | T/A;C | snv | 4 | |||
rs1185567 | 0.925 | 0.120 | 6 | 25818360 | intron variant | A/G;T | snv | 4 | |||
rs12215823 | 0.925 | 0.120 | 6 | 25725846 | upstream gene variant | G/C;T | snv | 4 | |||
rs13023194 | 0.925 | 0.120 | 2 | 27744393 | intergenic variant | G/A;C | snv | 4 | |||
rs1436306 | 0.925 | 0.120 | 6 | 25948193 | intergenic variant | A/G;T | snv | 4 |