Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10075801 | 5 | 132341949 | intron variant | A/G | snv | 0.31 | 5 | ||||
rs10138752 | 14 | 68713254 | intron variant | C/T | snv | 8.8E-02 | 5 | ||||
rs10206089 | 2 | 61476184 | intron variant | G/A | snv | 4 | |||||
rs10995477 | 10 | 63250912 | intron variant | T/C | snv | 0.43 | 4 | ||||
rs11204682 | 1 | 150623061 | intron variant | G/A;T | snv | 4 | |||||
rs112505971 | 10 | 27068541 | intron variant | A/C;G | snv | 13 | |||||
rs113473633 | 1.000 | 0.040 | 4 | 102527974 | intron variant | A/G | snv | 1.6E-02 | 4 | ||
rs11359909 | 3 | 128603031 | intergenic variant | G/- | delins | 0.89 | 4 | ||||
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 | ||||
rs11725704 | 4 | 74094279 | downstream gene variant | A/G | snv | 0.28 | 5 | ||||
rs12101888 | 15 | 41939155 | intron variant | C/T | snv | 0.34 | 3 | ||||
rs12239046 | 1 | 247438293 | intron variant | T/C | snv | 0.58 | 9 | ||||
rs12266014 | 10 | 24922362 | intron variant | C/T | snv | 0.26 | 7 | ||||
rs12450688 | 17 | 39987976 | intron variant | G/A | snv | 0.56 | 3 | ||||
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 | |||||
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 81 | |
rs13033745 | 2 | 66433271 | intron variant | G/T | snv | 0.67 | 2 | ||||
rs13138355 | 4 | 82624823 | upstream gene variant | C/A;T | snv | 4 | |||||
rs13331259 | 16 | 249924 | intron variant | A/G | snv | 3.0E-02 | 14 | ||||
rs139707092 | 2 | 168850753 | intron variant | TCTCTGGAAT/-;TCTCTGGAATTCTCTGGAAT | delins | 5 | |||||
rs143034248 | 11 | 118210555 | missense variant | C/T | snv | 4.0E-03 | 3.5E-03 | 7 |