Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7169629 | 15 | 84648043 | non coding transcript exon variant | C/G | snv | 0.51 | 1 | ||||
rs35258188 | 1.000 | 0.040 | 15 | 53705141 | missense variant | T/G | snv | 3.5E-03 | 1.5E-02 | 4 | |
rs17730281 | 1.000 | 0.080 | 15 | 53615751 | missense variant | G/A | snv | 0.26 | 0.22 | 3 | |
rs1906436 | 1.000 | 0.040 | 15 | 53590245 | intron variant | T/C | snv | 0.32 | 3 | ||
rs491567 | 1.000 | 0.080 | 15 | 53654396 | intron variant | A/C | snv | 0.34 | 3 | ||
rs10518732 | 15 | 53646845 | intron variant | G/A;C | snv | 2 | |||||
rs1031755 | 15 | 53659238 | intron variant | A/C | snv | 0.22 | 1 | ||||
rs10851543 | 15 | 53670551 | intron variant | A/G | snv | 0.32 | 1 | ||||
rs35255404 | 15 | 53627029 | intron variant | G/A | snv | 0.21 | 1 | ||||
rs5812700 | 15 | 53629192 | intron variant | AGAGAG/-;AG;AGAG;AGAGAGAG;AGAGAGAGAG;AGAGAGAGAGAG;AGAGAGAGAGAGAG | delins | 1 | |||||
rs62005941 | 15 | 53623569 | intron variant | C/A;G | snv | 1 | |||||
rs690428 | 15 | 53658381 | intron variant | A/C | snv | 0.35 | 1 | ||||
rs7169329 | 15 | 53610429 | intron variant | C/G | snv | 0.62 | 1 | ||||
rs10794720 | 1.000 | 0.080 | 10 | 1110225 | intron variant | T/C | snv | 0.89 | 3 | ||
rs3775932 | 4 | 10089306 | intron variant | C/A | snv | 0.47 | 1 | ||||
rs538063388 | 22 | 42049977 | intron variant | AAAAAAAAAAAAAAA/-;A;AA;AAA;AAAAAA;AAAAAAA;AAAAAAAA;AAAAAAAAA;AAAAAAAAAA;AAAAAAAAAAA;AAAAAAAAAAAA;AAAAAAAAAAAAA;AAAAAAAAAAAAAA;AAAAAAAAAAAAAAAA;AAAAAAAAAAAAAAAAA;AAAAAAAAAAAAAAAAAA;AAAAAAAAAAAAAAAAAAA;AAAAAAAAAAAAAAAAAAAA | delins | 9.2E-02 | 1 | ||||
rs284859 | 10 | 102813260 | missense variant | G/A;T | snv | 8.1E-06; 0.20 | 1 | ||||
rs6892 | 10 | 102816113 | 3 prime UTR variant | A/G | snv | 0.15 | 1 | ||||
rs55773927 | 7 | 65872915 | upstream gene variant | T/C;G | snv | 1 | |||||
rs17462630 | 2 | 218421818 | intron variant | G/A;C | snv | 0.24 | 1 | ||||
rs138551969 | 1.000 | 0.040 | 6 | 43780749 | missense variant | A/G | snv | 1.2E-05 | 3.5E-05 | 4 | |
rs11100781 | 4 | 143211469 | intron variant | A/G;T | snv | 1 | |||||
rs988911 | 2 | 61380375 | intron variant | G/A;T | snv | 0.19; 4.3E-06 | 1 | ||||
rs6589750 | 11 | 119456016 | intron variant | G/A | snv | 0.58 | 1 | ||||
rs17818393 | 2 | 209989752 | intron variant | A/G | snv | 0.51 | 1 |