Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2708861 | 0.851 | 0.120 | 7 | 47977120 | intron variant | T/G | snv | 0.46 | 6 | ||
rs771386507 | 0.882 | 0.120 | 6 | 31355479 | missense variant | C/T | snv | 4.0E-06 | 6 | ||
rs1456079929 | 0.851 | 0.120 | 11 | 101042001 | missense variant | C/A | snv | 8.0E-06 | 5 | ||
rs540432391 | 0.882 | 0.120 | 19 | 49043993 | 5 prime UTR variant | G/A;C | snv | 5 | |||
rs7246045 | 0.882 | 0.120 | 19 | 49042825 | upstream gene variant | T/G | snv | 2.9E-02 | 5 | ||
rs755378873 | 0.851 | 0.120 | 17 | 6694197 | missense variant | C/A;T | snv | 4.0E-06 | 5 | ||
rs10088218 | 0.851 | 0.120 | 8 | 128531703 | intron variant | G/A | snv | 0.13 | 4 | ||
rs11084033 | 0.882 | 0.120 | 19 | 50850699 | intron variant | C/A;T | snv | 4 | |||
rs11782652 | 0.851 | 0.120 | 8 | 81741409 | intron variant | A/G | snv | 6.6E-02 | 4 | ||
rs121913322 | 0.882 | 0.120 | 19 | 1221320 | missense variant | C/A;G;T | snv | 2.9E-05; 1.2E-04 | 4 | ||
rs1444192401 | 0.882 | 0.120 | 12 | 52235347 | missense variant | G/A | snv | 4 | |||
rs185229225 | 0.851 | 0.120 | 4 | 13607505 | intron variant | T/C | snv | 4 | |||
rs2072590 | 0.851 | 0.120 | 2 | 176177905 | non coding transcript exon variant | A/C;T | snv | 4 | |||
rs2287498 | 0.882 | 0.120 | 17 | 7689242 | synonymous variant | C/T | snv | 0.13 | 0.14 | 4 | |
rs495139 | 0.882 | 0.120 | 18 | 676008 | intron variant | G/C | snv | 0.63 | 4 | ||
rs4988344 | 0.882 | 0.120 | 17 | 61847251 | intron variant | G/C | snv | 0.20 | 0.15 | 4 | |
rs67164370 | 0.851 | 0.120 | 20 | 4787830 | intron variant | -/AGGGACT | ins | 4 | |||
rs6785617 | 0.882 | 0.120 | 3 | 172501054 | downstream gene variant | A/T | snv | 3.7E-02 | 4 | ||
rs7313833 | 0.851 | 0.120 | 12 | 27930263 | intergenic variant | G/A | snv | 0.37 | 4 | ||
rs74315464 | 0.882 | 0.120 | 22 | 50627048 | missense variant | G/A;C | snv | 4 | |||
rs10098821 | 0.882 | 0.120 | 8 | 128546982 | intron variant | C/T | snv | 7.6E-02 | 3 | ||
rs1136905 | 0.882 | 0.120 | 6 | 32518660 | missense variant | T/A;C | snv | 4.2E-03 | 3 | ||
rs11683487 | 0.882 | 0.120 | 2 | 151286035 | intron variant | G/T | snv | 0.36 | 3 | ||
rs121964872 | 0.882 | 0.120 | 16 | 68833362 | missense variant | A/G | snv | 4.4E-05 | 1.1E-04 | 3 | |
rs13063604 | 0.882 | 0.120 | 3 | 128085887 | intron variant | G/A | snv | 0.23 | 3 |