Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs8321 | 0.742 | 0.320 | 6 | 30064745 | 3 prime UTR variant | A/C | snv | 5.4E-02 | 5.9E-02 | 15 | |
rs10484554 | 0.807 | 0.200 | 6 | 31306778 | intron variant | C/T | snv | 0.12 | 8 | ||
rs9264942 | 0.763 | 0.400 | 6 | 31306603 | intron variant | T/C | snv | 0.34 | 7 | ||
rs11157436 | 0.851 | 0.040 | 14 | 22168978 | synonymous variant | C/T | snv | 0.19 | 7 | ||
rs143633948 | 0.882 | 0.080 | 6 | 131504454 | intron variant | G/A;C | snv | 6 | |||
rs73132848 | 0.882 | 0.080 | 3 | 8764738 | intron variant | G/A | snv | 9.3E-02 | 6 | ||
rs1015164 | 0.925 | 3 | 46410189 | intron variant | A/C;G;T | snv | 6 | ||||
rs2442719 | 0.882 | 0.120 | 6 | 31352761 | intron variant | C/T | snv | 0.53 | 6 | ||
rs35897606 | 0.882 | 0.080 | 11 | 33436311 | intron variant | A/G | snv | 4.4E-02 | 6 | ||
rs79709413 | 0.882 | 0.080 | 13 | 24740488 | upstream gene variant | G/T | snv | 4.7E-02 | 6 | ||
rs73084982 | 0.882 | 0.080 | 20 | 3430406 | intergenic variant | G/A | snv | 3.5E-02 | 6 | ||
rs11790131 | 0.882 | 0.080 | 9 | 19469848 | intergenic variant | G/A;T | snv | 6 | |||
rs35467001 | 0.882 | 0.080 | 17 | 73383923 | missense variant | G/A | snv | 5.3E-02 | 6.3E-02 | 6 | |
rs4986790 | 0.438 | 0.800 | 9 | 117713024 | missense variant | A/G;T | snv | 6.1E-02; 4.0E-06 | 6 | ||
rs11231017 | 0.925 | 11 | 62293877 | downstream gene variant | G/A | snv | 0.29 | 5 | |||
rs13064773 | 0.925 | 3 | 158893105 | intergenic variant | G/A | snv | 0.39 | 5 | |||
rs16823858 | 0.925 | 3 | 115559835 | intron variant | G/A;C | snv | 5 | ||||
rs17151904 | 0.925 | 7 | 25568789 | TF binding site variant | G/A;C | snv | 5 | ||||
rs6594357 | 0.925 | 5 | 109205522 | intergenic variant | T/A;C | snv | 5 | ||||
rs6723162 | 0.925 | 2 | 70875156 | intergenic variant | A/T | snv | 0.65 | 5 | |||
rs7458938 | 0.925 | 7 | 125820594 | intergenic variant | G/A | snv | 0.72 | 5 | |||
rs17038463 | 0.925 | 3 | 1383484 | intron variant | T/C;G | snv | 5 | ||||
rs10808739 | 0.882 | 8 | 64727703 | intron variant | G/A | snv | 0.24 | 5 | |||
rs12460243 | 0.925 | 19 | 8066356 | intron variant | G/A | snv | 0.14 | 5 | |||
rs17691394 | 0.925 | 7 | 126684537 | intron variant | A/G | snv | 0.13 | 5 |