Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs5880 | 0.827 | 0.040 | 16 | 56981179 | missense variant | G/C | snv | 5.2E-02 | 3.7E-02 | 10 | |
rs114694170 | 1.000 | 0.040 | 5 | 88884379 | non coding transcript exon variant | T/C | snv | 3.6E-02 | 5 | ||
rs10761741 | 1.000 | 0.040 | 10 | 63306426 | intron variant | G/T | snv | 0.38 | 4 | ||
rs12817819 | 0.882 | 0.040 | 12 | 89645549 | intron variant | C/T | snv | 9.4E-02 | 3 | ||
rs4782371 | 1.000 | 0.040 | 16 | 88502423 | intron variant | T/A;G | snv | 3 | |||
rs1740073 | 1.000 | 0.040 | 6 | 43979661 | regulatory region variant | T/C | snv | 0.67 | 2 | ||
rs2375981 | 1.000 | 0.040 | 9 | 2692583 | regulatory region variant | C/G;T | snv | 2 | |||
rs2639990 | 1.000 | 0.040 | 18 | 75203596 | intron variant | T/C | snv | 0.12 | 2 | ||
rs7043199 | 1.000 | 0.040 | 9 | 2621145 | intron variant | T/A | snv | 0.18 | 2 | ||
rs884164 | 0.925 | 0.040 | 19 | 4521613 | upstream gene variant | A/G;T | snv | 2 | |||
rs138880920 | 1.000 | 0.040 | 9 | 104826957 | missense variant | C/G | snv | 3.3E-03 | 1.8E-03 | 1 | |
rs33918808 | 1.000 | 0.040 | 9 | 104817351 | missense variant | C/G;T | snv | 3.5E-02; 4.0E-06 | 1 | ||
rs3917643 | 1.000 | 0.040 | 1 | 94536311 | intron variant | T/C | snv | 3.9E-02 | 1 | ||
rs6993770 | 0.925 | 0.080 | 8 | 105569300 | intron variant | A/T | snv | 0.31 | 9 | ||
rs11234027 | 0.882 | 0.080 | 11 | 71523061 | intron variant | G/A | snv | 0.24 | 5 | ||
rs1144507 | 0.925 | 0.080 | 11 | 123729767 | missense variant | A/C;G;T | snv | 0.68 | 2 | ||
rs17057255 | 0.925 | 0.080 | 8 | 27503724 | missense variant | C/T | snv | 1.3E-02 | 3.4E-02 | 2 | |
rs17105278 | 0.925 | 0.080 | 14 | 68261762 | intron variant | T/C | snv | 0.36 | 2 | ||
rs281860391 | 0.925 | 0.080 | 6 | 31271690 | stop gained | C/T | snv | 2 | |||
rs750249283 | 0.925 | 0.080 | 21 | 42296256 | missense variant | C/G;T | snv | 4.0E-06; 8.0E-06 | 2 | ||
rs872129 | 0.925 | 0.080 | 1 | 203200263 | intergenic variant | A/G | snv | 0.19 | 2 | ||
rs147377392 | 0.763 | 0.120 | 20 | 23048144 | missense variant | A/G | snv | 1.0E-04 | 2.8E-04 | 11 | |
rs12713559 | 0.776 | 0.120 | 2 | 21006196 | missense variant | G/A | snv | 3.4E-04 | 5.0E-04 | 10 | |
rs544456198 | 0.790 | 0.120 | 19 | 11116930 | missense variant | G/T | snv | 8.0E-06 | 2.8E-05 | 9 | |
rs2066718 | 0.882 | 0.120 | 9 | 104826974 | missense variant | C/G;T | snv | 4.3E-04; 5.4E-02 | 7 |