Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11597086 | 10 | 100193948 | non coding transcript exon variant | A/C | snv | 0.30 | 0.29 | 1 | |||
rs17883880 | 10 | 100230590 | intron variant | T/A | snv | 1.2E-02 | 4 | ||||
rs11224571 | 11 | 101047942 | intron variant | C/A | snv | 1.2E-02 | 3 | ||||
rs7928851 | 11 | 101117160 | intron variant | C/A | snv | 1.7E-02 | 3 | ||||
rs11571151 | 11 | 101127486 | missense variant | C/G;T | snv | 6 | |||||
rs12097137 | 1 | 101243889 | downstream gene variant | G/A;T | snv | 3 | |||||
rs12101753 | 15 | 101446855 | intron variant | T/C | snv | 4.3E-02 | 1 | ||||
rs28385681 | 2 | 102017062 | intron variant | T/G | snv | 1.4E-05 | 1 | ||||
rs3917237 | 2 | 102155991 | intron variant | G/A | snv | 1.9E-02 | 1 | ||||
rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 8 | ||
rs7952037 | 11 | 102379653 | downstream gene variant | C/T | snv | 1.9E-02 | 3 | ||||
rs5030339 | 19 | 10269461 | intron variant | G/A | snv | 3.4E-03 | 5 | ||||
rs5030359 | 19 | 10277786 | intron variant | G/A | snv | 2.1E-03 | 3 | ||||
rs7938449 | 11 | 102778167 | intron variant | C/A;T | snv | 1 | |||||
rs11760826 | 7 | 103151364 | upstream gene variant | A/C;G | snv | 1 | |||||
rs1997243 | 7 | 1044141 | intron variant | A/G | snv | 0.11 | 1 | ||||
rs9282541 | 0.790 | 0.160 | 9 | 104858554 | missense variant | G/A | snv | 1.3E-02 | 4.4E-03 | 2 | |
rs4149273 | 9 | 104879930 | intron variant | T/C | snv | 0.45 | 3 | ||||
rs4149272 | 9 | 104880006 | intron variant | C/G;T | snv | 0.48 | 3 | ||||
rs11789603 | 9 | 104884738 | intron variant | C/T | snv | 0.11 | 2 | ||||
rs4149269 | 9 | 104884840 | intron variant | A/G | snv | 0.41 | 3 | ||||
rs4149268 | 1.000 | 0.040 | 9 | 104884939 | intron variant | C/T | snv | 0.46 | 4 | ||
rs3890182 | 0.925 | 0.120 | 9 | 104885374 | intron variant | G/A;T | snv | 4 | |||
rs3847300 | 9 | 104886149 | intron variant | G/A | snv | 0.12 | 3 | ||||
rs13290420 | 9 | 104886684 | intron variant | T/C | snv | 0.16 | 3 |