Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10405744 | 0.851 | 0.040 | 19 | 19948684 | intron variant | G/A | snv | 9.0E-02 | 4 | ||
rs10503253 | 0.851 | 0.040 | 8 | 4323322 | intron variant | C/A | snv | 0.18 | 5 | ||
rs1054442 | 0.925 | 0.040 | 12 | 48995537 | 3 prime UTR variant | A/C | snv | 0.46 | 4 | ||
rs105633 | 0.882 | 0.040 | 5 | 141945684 | synonymous variant | T/C;G | snv | 0.98; 4.0E-06 | 3 | ||
rs10774037 | 0.882 | 0.040 | 12 | 2311360 | intron variant | G/A | snv | 0.77 | 3 | ||
rs10968749 | 0.851 | 0.040 | 9 | 28752486 | intergenic variant | A/G | snv | 5.5E-02 | 4 | ||
rs10994359 | 0.827 | 0.040 | 10 | 60462349 | intron variant | T/C | snv | 8.0E-02 | 5 | ||
rs10994397 | 0.851 | 0.040 | 10 | 60519366 | intron variant | C/T | snv | 9.5E-02 | 5 | ||
rs11004733 | 0.882 | 0.040 | 10 | 55089584 | intron variant | C/T | snv | 2.9E-02 | 4 | ||
rs11125080 | 0.882 | 0.040 | 2 | 46505266 | intron variant | G/A;C | snv | 3 | |||
rs11152369 | 0.851 | 0.040 | 18 | 55399097 | intron variant | A/C | snv | 6.3E-02 | 5 | ||
rs11191580 | 0.827 | 0.040 | 10 | 103146454 | intron variant | T/C | snv | 7.9E-02 | 12 | ||
rs115777110 | 0.882 | 0.040 | 1 | 208936211 | intergenic variant | T/C | snv | 1.2E-02 | 3 | ||
rs11829119 | 0.851 | 0.040 | 12 | 19040597 | intergenic variant | T/A;C | snv | 4 | |||
rs12052005 | 0.882 | 0.040 | 18 | 68832311 | intron variant | G/C;T | snv | 3 | |||
rs12325410 | 0.851 | 0.040 | 16 | 9581389 | intron variant | T/G | snv | 0.16 | 5 | ||
rs12443954 | 0.851 | 0.040 | 16 | 89675088 | intron variant | A/C;G | snv | 5 | |||
rs12871532 | 0.851 | 0.040 | 13 | 108016199 | intergenic variant | T/C | snv | 0.46 | 5 | ||
rs12966547 | 0.827 | 0.040 | 18 | 55084786 | intergenic variant | G/A | snv | 0.39 | 5 | ||
rs13001243 | 0.882 | 0.040 | 2 | 234306004 | regulatory region variant | G/A | snv | 7.5E-02 | 3 | ||
rs13072940 | 0.851 | 0.040 | 3 | 36801132 | regulatory region variant | T/A | snv | 0.37 | 5 | ||
rs13418455 | 0.851 | 0.040 | 2 | 180212022 | intergenic variant | C/T | snv | 0.29 | 5 | ||
rs137928907 | 0.882 | 0.040 | 12 | 130827204 | missense variant | A/C | snv | 1.4E-02 | 1.5E-02 | 3 | |
rs138449918 | 0.882 | 0.040 | 2 | 39936810 | intron variant | AT/-;ATAT | delins | 3 | |||
rs141252918 | 0.882 | 0.040 | 6 | 151506923 | intron variant | G/A;C | snv | 4 |