Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs147233090 | 0.925 | 0.040 | 15 | 43735849 | intron variant | C/T | snv | 1.7E-02 | 6 | ||
rs1505307 | 3 | 24301839 | intron variant | T/C | snv | 0.60 | 6 | ||||
rs17534202 | 1.000 | 0.120 | 1 | 203312047 | downstream gene variant | G/C | snv | 0.40 | 6 | ||
rs2979489 | 8 | 30423317 | intron variant | G/A;C | snv | 6 | |||||
rs35158985 | 0.882 | 0.080 | 16 | 68762843 | intron variant | A/G | snv | 0.38 | 6 | ||
rs7203560 | 1.000 | 0.080 | 16 | 134391 | intron variant | T/G | snv | 2.0E-02 | 6 | ||
rs737092 | 20 | 57415349 | regulatory region variant | T/C | snv | 0.58 | 6 | ||||
rs7385804 | 0.851 | 0.120 | 7 | 100638347 | intron variant | C/A | snv | 0.65 | 6 | ||
rs9349205 | 6 | 41957421 | intron variant | G/A;C | snv | 6 | |||||
rs9399137 | 0.851 | 0.320 | 6 | 135097880 | intron variant | T/C | snv | 0.20 | 6 | ||
rs10858740 | 12 | 88451258 | intergenic variant | A/G;T | snv | 0.56 | 5 | ||||
rs112233623 | 6 | 41957260 | intron variant | C/T | snv | 7.0E-03 | 5 | ||||
rs113542380 | 2 | 43237679 | intron variant | G/A | snv | 4.7E-02 | 5 | ||||
rs11627485 | 14 | 65020976 | intron variant | T/C | snv | 0.36 | 5 | ||||
rs13339636 | 16 | 248589 | intron variant | A/G | snv | 3.8E-02 | 5 | ||||
rs1434282 | 1 | 199041592 | non coding transcript exon variant | C/T | snv | 0.76 | 5 | ||||
rs1569419 | 1 | 3080038 | intron variant | T/C | snv | 0.73 | 5 | ||||
rs218237 | 4 | 54528005 | intergenic variant | C/T | snv | 0.18 | 5 | ||||
rs2294915 | 1.000 | 0.040 | 22 | 43945024 | intron variant | C/G;T | snv | 5 | |||
rs2413450 | 22 | 37074184 | intron variant | T/C | snv | 0.61 | 5 | ||||
rs3218097 | 6 | 41937537 | intron variant | G/A;T | snv | 5 | |||||
rs3768321 | 1.000 | 0.080 | 1 | 39570256 | intron variant | G/T | snv | 0.14 | 5 | ||
rs3809627 | 16 | 30091839 | 5 prime UTR variant | C/A | snv | 0.41 | 5 | ||||
rs4449583 | 5 | 1284020 | intron variant | C/T | snv | 0.25 | 5 | ||||
rs532398216 | 16 | 182398 | downstream gene variant | TGAG/- | delins | 2.0E-03 | 5 |