Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 34 | |
rs6679677 | 0.653 | 0.320 | 1 | 113761186 | upstream gene variant | C/A | snv | 6.7E-02 | 25 | ||
rs11580078 | 0.724 | 0.240 | 1 | 67203951 | intron variant | C/A;G | snv | 14 | |||
rs2066363 | 0.724 | 0.240 | 1 | 81771892 | intron variant | C/T | snv | 0.71 | 14 | ||
rs34884278 | 0.724 | 0.240 | 1 | 172869708 | intron variant | C/T | snv | 0.63 | 14 | ||
rs55705316 | 0.724 | 0.240 | 1 | 206760172 | regulatory region variant | T/A;G | snv | 14 | |||
rs6689858 | 0.724 | 0.240 | 1 | 197406337 | intron variant | T/C | snv | 0.39 | 14 | ||
rs11209026 | 0.597 | 0.680 | 1 | 67240275 | missense variant | G/A | snv | 4.2E-02 | 4.6E-02 | 5 | |
rs17849502 | 0.827 | 0.240 | 1 | 183563445 | missense variant | G/A;C;T | snv | 4.0E-06; 4.0E-06; 3.4E-02 | 5 | ||
rs864537 | 0.925 | 0.200 | 1 | 167442147 | intron variant | A/G | snv | 0.29 | 3 | ||
rs12068671 | 0.925 | 0.160 | 1 | 172711891 | intergenic variant | T/C | snv | 0.23 | 2 | ||
rs12734338 | 0.925 | 0.120 | 1 | 202500595 | intron variant | T/C | snv | 2 | |||
rs1359062 | 0.925 | 0.160 | 1 | 192572342 | intron variant | C/A;G;T | snv | 2 | |||
rs3748816 | 0.827 | 0.200 | 1 | 2595307 | missense variant | A/G | snv | 0.41 | 0.46 | 2 | |
rs4073285 | 0.925 | 0.200 | 1 | 2608357 | intron variant | C/T | snv | 0.40 | 2 | ||
rs6696533 | 0.925 | 0.200 | 1 | 198764438 | intergenic variant | T/C | snv | 0.28 | 2 | ||
rs10800746 | 1.000 | 0.080 | 1 | 200912264 | intron variant | C/T | snv | 0.32 | 1 | ||
rs10903122 | 0.882 | 0.200 | 1 | 24977085 | intergenic variant | A/G | snv | 0.56 | 1 | ||
rs12142280 | 1.000 | 0.080 | 1 | 172895512 | intron variant | T/A | snv | 0.21 | 1 | ||
rs12727642 | 1.000 | 0.080 | 1 | 7986612 | upstream gene variant | C/A | snv | 0.12 | 1 | ||
rs2157453 | 1.000 | 0.080 | 1 | 172894808 | intron variant | G/A | snv | 0.31 | 1 | ||
rs2816316 | 0.882 | 0.200 | 1 | 192567683 | intron variant | C/A | snv | 0.79 | 1 | ||
rs296547 | 0.882 | 0.200 | 1 | 200923009 | intron variant | T/C | snv | 0.53 | 1 | ||
rs4445406 | 1.000 | 0.080 | 1 | 2607961 | intron variant | T/C | snv | 0.41 | 1 | ||
rs59655222 | 1.000 | 0.080 | 1 | 200906769 | intron variant | T/C | snv | 0.22 | 1 |