Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11655505 | 0.776 | 0.160 | 17 | 43126360 | intron variant | G/A | snv | 0.31 | 8 | ||
rs1467465 | 0.827 | 0.160 | 1 | 27884892 | non coding transcript exon variant | A/G | snv | 0.61 | 7 | ||
rs1800709 | 0.851 | 0.160 | 17 | 43093010 | missense variant | G/A | snv | 1.7E-03 | 1.4E-03 | 6 | |
rs1800751 | 0.851 | 0.160 | 17 | 43047676 | missense variant | G/A;C | snv | 4.0E-06 | 5 | ||
rs190900046 | 0.827 | 0.160 | 17 | 43104197 | synonymous variant | A/C | snv | 8.0E-06 | 4.2E-05 | 5 | |
rs2363956 | 0.776 | 0.160 | 19 | 17283315 | missense variant | T/G | snv | 0.48 | 0.50 | 8 | |
rs2665390 | 0.776 | 0.160 | 3 | 156679960 | intron variant | C/T | snv | 0.92 | 8 | ||
rs273900729 | 0.925 | 0.160 | 17 | 43082529 | missense variant | A/G | snv | 2 | |||
rs28997576 | 0.776 | 0.160 | 2 | 214752454 | missense variant | C/G;T | snv | 1.5E-02 | 11 | ||
rs3177427 | 0.827 | 0.160 | 14 | 77326864 | stop gained | G/A;C;T | snv | 5 | |||
rs372038369 | 0.882 | 0.160 | 17 | 35101233 | missense variant | G/A;T | snv | 1.2E-05 | 1.4E-05 | 3 | |
rs41293521 | 0.925 | 0.160 | 13 | 32394724 | missense variant | T/C | snv | 2.9E-04 | 2.5E-04 | 2 | |
rs4987046 | 0.925 | 0.160 | 13 | 32319134 | missense variant | A/G | snv | 1.6E-03 | 1.6E-03 | 4 | |
rs56307747 | 0.776 | 0.160 | 7 | 74059952 | missense variant | G/A;C | snv | 4.0E-06 | 8 | ||
rs587780128 | 0.882 | 0.160 | 7 | 152649010 | missense variant | G/A | snv | 1.2E-05 | 3.5E-05 | 3 | |
rs587782818 | 0.790 | 0.160 | 17 | 58703325 | stop gained | C/G | snv | 6.4E-05; 4.0E-06 | 1.4E-05 | 8 | |
rs61755649 | 0.882 | 0.160 | 14 | 67885891 | missense variant | C/T | snv | 6.8E-05 | 4.9E-05 | 3 | |
rs638820 | 0.827 | 0.160 | 1 | 109667284 | intron variant | G/A | snv | 0.52 | 5 | ||
rs67397200 | 0.827 | 0.160 | 19 | 17290595 | upstream gene variant | C/G | snv | 0.27 | 5 | ||
rs748876625 | 0.807 | 0.160 | 17 | 43104122 | missense variant | C/A;G | snv | 1.2E-05 | 10 | ||
rs750042441 | 0.827 | 0.160 | 11 | 101128367 | missense variant | G/A;C | snv | 6.1E-05; 4.3E-06 | 5 | ||
rs764918809 | 0.827 | 0.160 | 12 | 68839337 | missense variant | T/C | snv | 4.0E-06 | 6 | ||
rs786203319 | 0.827 | 0.160 | 17 | 43115759 | missense variant | G/A | snv | 6 | |||
rs80356897 | 0.827 | 0.160 | 17 | 43099853 | missense variant | A/G | snv | 5 | |||
rs80359078 | 0.882 | 0.160 | 13 | 32370430 | missense variant | G/A | snv | 3.2E-05 | 2.1E-05 | 3 |