Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs653178 | 0.672 | 0.600 | 12 | 111569952 | intron variant | C/T | snv | 0.67 | 17 | ||
rs687289 | 1.000 | 0.120 | 9 | 133261703 | intron variant | A/G | snv | 9 | |||
rs687621 | 0.851 | 0.240 | 9 | 133261662 | intron variant | G/A;C | snv | 9 | |||
rs12075 | 0.724 | 0.240 | 1 | 159205564 | missense variant | G/A | snv | 0.51 | 0.66 | 3 | |
rs2814778 | 0.763 | 0.360 | 1 | 159204893 | 5 prime UTR variant | T/C | snv | 0.25 | 3 | ||
rs7578982 | 2 | 111078961 | intron variant | T/C | snv | 0.27 | 2 | ||||
rs445 | 7 | 92779056 | intron variant | C/T | snv | 0.14 | 2 | ||||
rs7776054 | 6 | 135097778 | intron variant | A/G | snv | 0.24 | 2 | ||||
rs10276619 | 1.000 | 0.080 | 7 | 50273756 | downstream gene variant | G/A | snv | 0.59 | 1 | ||
rs11611647 | 12 | 4224753 | intergenic variant | T/C | snv | 0.22 | 1 | ||||
rs12711490 | 0.925 | 0.080 | 16 | 85939422 | intron variant | T/C | snv | 0.18 | 1 | ||
rs1449263 | 1.000 | 0.080 | 2 | 181454574 | upstream gene variant | C/T | snv | 0.56 | 1 | ||
rs3095254 | 6 | 31253891 | intergenic variant | C/A;G | snv | 0.55 | 1 | ||||
rs913678 | 0.882 | 0.240 | 20 | 50338887 | regulatory region variant | T/C | snv | 0.51 | 1 | ||
rs9880192 | 1.000 | 0.040 | 3 | 128578726 | upstream gene variant | G/A;C | snv | 0.31 | 1 | ||
rs2228468 | 0.882 | 0.120 | 3 | 42865620 | missense variant | A/C;T | snv | 0.43; 8.3E-03 | 1 | ||
rs10098310 | 8 | 129601368 | intron variant | G/A;T | snv | 1 | |||||
rs10956483 | 8 | 129559864 | intron variant | G/A;C | snv | 1 | |||||
rs1991866 | 8 | 129611859 | intron variant | G/A;C | snv | 1 | |||||
rs3731211 | 9 | 21986848 | intron variant | T/A | snv | 0.74 | 1 | ||||
rs334 | 0.724 | 0.240 | 11 | 5227002 | missense variant | T/A;C;G | snv | 3.5E-03 | 1 | ||
rs2292982 | 1.000 | 0.120 | 16 | 85911217 | intron variant | T/C;G | snv | 1 | |||
rs12988934 | 2 | 181458938 | non coding transcript exon variant | C/T | snv | 5.9E-02 | 1 | ||||
rs6584283 | 0.776 | 0.080 | 10 | 99530544 | intron variant | T/C | snv | 0.56 | 1 | ||
rs11190141 | 1.000 | 0.040 | 10 | 99532633 | upstream gene variant | C/T | snv | 0.40 | 1 |