Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs572842823 | 0.763 | 0.160 | 21 | 25897626 | missense variant | T/A;G | snv | 11 | |||
rs371425292 | 0.763 | 0.160 | 21 | 25897627 | missense variant | C/A;T | snv | 8.0E-06 | 10 | ||
rs28936379 | 0.807 | 0.120 | 1 | 226888977 | missense variant | A/C;G;T | snv | 4.0E-06 | 10 | ||
rs1386984902 | 0.790 | 0.160 | 21 | 26000095 | missense variant | G/A | snv | 9 | |||
rs1108580 | 0.790 | 0.240 | 9 | 133639992 | splice region variant | A/G | snv | 0.45 | 0.54 | 9 | |
rs387906709 | 0.776 | 0.120 | X | 56565363 | missense variant | C/A;T | snv | 9 | |||
rs1223904774 | 0.790 | 0.120 | 21 | 25891772 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 8 | |
rs121909668 | 0.790 | 0.120 | 16 | 31191418 | missense variant | C/A;G;T | snv | 1.2E-05 | 8 | ||
rs10748842 | 0.807 | 0.120 | 10 | 81889983 | intron variant | T/C | snv | 0.13 | 8 | ||
rs77369218 | 0.807 | 0.160 | 1 | 155235726 | missense variant | T/A | snv | 7 | |||
rs7157599 | 0.925 | 0.040 | 14 | 100159565 | missense variant | C/T | snv | 0.73 | 0.76 | 6 | |
rs1018381 | 0.882 | 0.040 | 6 | 15656839 | intron variant | G/A | snv | 0.16 | 6 | ||
rs75548401 | 0.882 | 0.160 | 1 | 155236246 | missense variant | G/A | snv | 5.9E-03 | 6.2E-03 | 6 | |
rs1329650 | 0.882 | 0.080 | 10 | 91588363 | regulatory region variant | G/A;T | snv | 6 | |||
rs6584400 | 0.851 | 0.120 | 10 | 81896770 | intron variant | G/A | snv | 0.22 | 6 | ||
rs8074995 | 0.925 | 0.040 | 17 | 66796013 | intron variant | G/A | snv | 0.13 | 5 | ||
rs2344484 | 0.925 | 0.040 | 5 | 135540941 | upstream gene variant | A/G | snv | 0.47 | 3 | ||
rs761715536 | 1.000 | 0.040 | 10 | 111079092 | stop gained | G/A;T | snv | 6.4E-06; 1.3E-05 | 3 | ||
rs1800557 | 0.925 | 0.040 | 21 | 25891795 | missense variant | G/A | snv | 4.0E-05 | 4.2E-05 | 3 | |
rs2189814 | 0.925 | 0.040 | 7 | 86702440 | intron variant | T/A;C | snv | 3 | |||
rs1315695444 | 1.000 | 0.040 | 1 | 169611580 | missense variant | C/G | snv | 4.0E-06 | 1.4E-05 | 2 | |
rs1245342105 | 1.000 | 0.040 | 2 | 54622367 | missense variant | T/C | snv | 4.0E-06 | 2 |