Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs114050631 | 2 | 218156235 | regulatory region variant | C/T | snv | 6.9E-03 | 5 | ||||
rs1144700 | 6 | 16744456 | intron variant | C/G;T | snv | 5 | |||||
rs11624512 | 14 | 92644775 | non coding transcript exon variant | C/T | snv | 0.15 | 5 | ||||
rs11654074 | 17 | 59748211 | intron variant | A/C | snv | 0.40 | 5 | ||||
rs11725704 | 4 | 74094279 | downstream gene variant | A/G | snv | 0.28 | 5 | ||||
rs12542907 | 8 | 67900953 | intergenic variant | C/G | snv | 0.29 | 5 | ||||
rs12550612 | 8 | 23109256 | intron variant | G/A | snv | 0.83 | 5 | ||||
rs12600856 | 17 | 40007042 | intergenic variant | T/C;G | snv | 5 | |||||
rs139707092 | 2 | 168850753 | intron variant | TCTCTGGAAT/-;TCTCTGGAATTCTCTGGAAT | delins | 5 | |||||
rs145013566 | 2 | 218297998 | intron variant | -/C | ins | 5 | |||||
rs146890554 | 17 | 40017384 | 3 prime UTR variant | C/T | snv | 9.6E-03 | 5 | ||||
rs147694761 | 18 | 23571654 | intron variant | AAAA/-;A;AA;AAA;AAAAA;AAAAAA | delins | 5 | |||||
rs16978075 | 18 | 44533186 | intron variant | T/C | snv | 8.5E-02 | 5 | ||||
rs192022 | 11 | 108378047 | intron variant | C/G;T | snv | 5 | |||||
rs1968252 | 19 | 7782850 | upstream gene variant | G/A;T | snv | 5 | |||||
rs1982094 | 8 | 129612570 | intron variant | C/T | snv | 4.8E-02 | 5 | ||||
rs200638392 | 6 | 87128241 | intergenic variant | GAT/-;GATGAT | delins | 0.47 | 5 | ||||
rs201950044 | 1 | 161639782 | intergenic variant | G/T | snv | 5 | |||||
rs2082382 | 5 | 148820990 | upstream gene variant | G/A | snv | 0.72 | 5 | ||||
rs2158799 | 7 | 28237488 | intron variant | C/G;T | snv | 0.70 | 5 | ||||
rs2208568 | 1 | 235926855 | intergenic variant | T/A;C;G | snv | 5 | |||||
rs2271400 | 8 | 55878685 | upstream gene variant | C/T | snv | 0.68 | 5 | ||||
rs2338224 | 5 | 72432861 | intergenic variant | A/G | snv | 0.85 | 5 | ||||
rs238914 | 11 | 114113387 | intron variant | C/A | snv | 0.45 | 5 | ||||
rs2846630 | 11 | 114086475 | intron variant | G/A | snv | 0.35 | 5 |