Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2278744 | 0.925 | 0.080 | 10 | 69392716 | intron variant | C/T | snv | 0.18 | 2 | ||
rs6856901 | 0.925 | 0.080 | 4 | 83295215 | 3 prime UTR variant | C/G | snv | 0.27 | 2 | ||
rs6968084 | 0.925 | 0.080 | 7 | 112457066 | missense variant | C/T | snv | 0.17 | 0.16 | 2 | |
rs4764887 | 0.925 | 0.080 | 12 | 102430122 | intron variant | G/A | snv | 2.2E-02 | 2 | ||
rs3748068 | 0.925 | 0.080 | 6 | 52190537 | 3 prime UTR variant | C/T | snv | 2 | |||
rs9382084 | 0.925 | 0.080 | 6 | 52240869 | intron variant | G/A;T | snv | 2 | |||
rs1135354 | 0.925 | 0.080 | 2 | 102397842 | 3 prime UTR variant | T/G | snv | 0.23 | 2 | ||
rs3771157 | 0.925 | 0.080 | 2 | 102396972 | 3 prime UTR variant | C/A | snv | 3.7E-02 | 2 | ||
rs3732131 | 0.925 | 0.080 | 2 | 102178143 | 3 prime UTR variant | A/G | snv | 0.12 | 2 | ||
rs2472188 | 0.925 | 0.080 | 2 | 113063237 | 3 prime UTR variant | C/G | snv | 0.65 | 2 | ||
rs2515401 | 0.882 | 0.080 | 2 | 113062899 | 3 prime UTR variant | T/A;C | snv | 2 | |||
rs2515402 | 0.925 | 0.080 | 2 | 113063003 | 3 prime UTR variant | C/A | snv | 0.65 | 2 | ||
rs3180235 | 0.882 | 0.080 | 2 | 113063095 | 3 prime UTR variant | A/G | snv | 0.65 | 2 | ||
rs957201 | 0.925 | 0.080 | 2 | 113063623 | 3 prime UTR variant | T/C | snv | 0.65 | 2 | ||
rs10421916 | 0.925 | 0.080 | 19 | 17818178 | intron variant | A/G | snv | 0.69 | 2 | ||
rs2447867 | 0.925 | 0.080 | 5 | 52861540 | missense variant | T/C;G | snv | 0.79; 4.0E-06 | 2 | ||
rs74483926 | 0.925 | 0.080 | 7 | 152162598 | missense variant | G/A | snv | 4.8E-02 | 3.4E-02 | 2 | |
rs11944405 | 0.925 | 0.080 | 4 | 99878804 | 3 prime UTR variant | T/C | snv | 0.28 | 2 | ||
rs1230025 | 0.925 | 0.080 | 4 | 99265219 | intron variant | A/G;T | snv | 2 | |||
rs3815254 | 0.925 | 0.080 | 7 | 19943391 | non coding transcript exon variant | T/C;G | snv | 2 | |||
rs28361491 | 0.925 | 0.080 | 4 | 44801181 | intergenic variant | C/A;T | snv | 2 | |||
rs34160967 | 0.925 | 0.080 | 1 | 6575246 | missense variant | G/A;C | snv | 0.13; 4.0E-06 | 2 | ||
rs579501 | 0.925 | 0.080 | 10 | 42751347 | non coding transcript exon variant | T/G | snv | 5.9E-02 | 2 | ||
rs73239138 | 0.925 | 0.080 | 4 | 66276902 | mature miRNA variant | G/A | snv | 0.27 | 0.36 | 2 | |
rs35010275 | 0.925 | 0.080 | 12 | 53991008 | intron variant | G/A;C | snv | 2 |