Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs53576 | 0.641 | 0.320 | 3 | 8762685 | intron variant | A/G;T | snv | 42 | |||
rs1042778 | 0.925 | 0.040 | 3 | 8752859 | 3 prime UTR variant | G/A;C;T | snv | 3 | |||
rs4564970 | 3 | 8768722 | intron variant | G/A;C | snv | 1 | |||||
rs3756007 | 1.000 | 0.080 | 4 | 46389047 | 5 prime UTR variant | T/C | snv | 5.4E-02 | 2 | ||
rs11215217 | 11 | 114818979 | intergenic variant | C/T | snv | 6.8E-02 | 1 | ||||
rs2119183 | 1.000 | 0.080 | 4 | 46270789 | intron variant | G/A | snv | 7.6E-02 | 2 | ||
rs11941860 | 1.000 | 0.080 | 4 | 46080161 | intron variant | C/T | snv | 0.12 | 2 | ||
rs17689918 | 0.851 | 0.080 | 17 | 45832722 | intron variant | G/A | snv | 0.15 | 6 | ||
rs12106331 | 21 | 37354975 | intron variant | A/G | snv | 0.17 | 1 | ||||
rs2835702 | 21 | 37352009 | intron variant | T/C | snv | 0.17 | 1 | ||||
rs6296 | 0.732 | 0.160 | 6 | 77462543 | synonymous variant | C/G | snv | 0.31 | 0.27 | 23 | |
rs7632287 | 1.000 | 0.040 | 3 | 8749760 | intron variant | G/A | snv | 0.32 | 2 | ||
rs9471290 | 6 | 40292776 | intergenic variant | G/A | snv | 0.38 | 1 | ||||
rs4680 | 0.442 | 0.920 | 22 | 19963748 | missense variant | G/A | snv | 0.46 | 0.44 | 249 | |
rs536599 | 1.000 | 0.080 | 4 | 46196917 | intergenic variant | G/T | snv | 0.47 | 2 | ||
rs346425 | 5 | 63300417 | upstream gene variant | T/C | snv | 0.48 | 1 | ||||
rs4714329 | 6 | 40305718 | intergenic variant | G/A | snv | 0.57 | 1 |