Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1002487 | 1 | 26539480 | intron variant | T/C | snv | 5.3E-02 | 1 | ||||
rs10033119 | 4 | 163324702 | 3 prime UTR variant | A/G | snv | 7.9E-02 | 1 | ||||
rs10047462 | 11 | 116851325 | intron variant | G/C;T | snv | 1 | |||||
rs10054063 | 5 | 173965395 | downstream gene variant | A/T | snv | 0.26 | 4 | ||||
rs1009360 | 2 | 65048915 | intron variant | T/C | snv | 0.51 | 2 | ||||
rs10096633 | 1.000 | 0.040 | 8 | 19973410 | regulatory region variant | C/T | snv | 0.22 | 2 | ||
rs10101067 | 8 | 71495139 | intron variant | G/C | snv | 6.2E-02 | 2 | ||||
rs10105606 | 8 | 19970337 | downstream gene variant | C/A | snv | 0.42 | 2 | ||||
rs10106652 | 1.000 | 0.040 | 8 | 20070649 | intergenic variant | G/A | snv | 0.29 | 3 | ||
rs1011731 | 1 | 172377408 | intron variant | G/A | snv | 0.46 | 4 | ||||
rs10119 | 0.925 | 0.080 | 19 | 44903416 | 3 prime UTR variant | G/A | snv | 0.28 | 1 | ||
rs10127775 | 1 | 230160042 | intron variant | A/G;T | snv | 4 | |||||
rs10152811 | 15 | 86311359 | intron variant | A/C | snv | 0.28 | 1 | ||||
rs10184004 | 1.000 | 0.080 | 2 | 164651879 | downstream gene variant | C/T | snv | 0.48 | 5 | ||
rs10185855 | 2 | 101025798 | intron variant | A/G | snv | 0.35 | 4 | ||||
rs10195252 | 0.925 | 0.080 | 2 | 164656581 | intron variant | T/C | snv | 0.48 | 6 | ||
rs10198175 | 0.925 | 0.080 | 2 | 20934123 | intergenic variant | A/G | snv | 0.93 | 2 | ||
rs10199914 | 2 | 238975165 | regulatory region variant | A/G | snv | 0.39 | 1 | ||||
rs102275 | 0.827 | 0.320 | 11 | 61790331 | non coding transcript exon variant | T/C | snv | 0.47 | 10 | ||
rs10281741 | 7 | 158000430 | intron variant | G/A;C;T | snv | 1 | |||||
rs1037814 | 4 | 87128698 | intron variant | T/C | snv | 0.60 | 2 | ||||
rs10401969 | 0.776 | 0.240 | 19 | 19296909 | intron variant | T/C | snv | 0.10 | 22 | ||
rs10402271 | 1.000 | 0.080 | 19 | 44825957 | downstream gene variant | T/G | snv | 0.28 | 4 | ||
rs10408163 | 19 | 47093845 | non coding transcript exon variant | T/C | snv | 0.52 | 6 | ||||
rs10417097 | 19 | 19609015 | intron variant | C/G | snv | 0.45 | 1 |