Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4841132 | 8 | 9326086 | non coding transcript exon variant | A/G | snv | 0.89 | 14 | ||||
rs217181 | 16 | 72080103 | intron variant | C/T | snv | 0.20 | 6 | ||||
rs2731672 | 5 | 177415473 | intron variant | T/C | snv | 0.66 | 6 | ||||
rs10127775 | 1 | 230160042 | intron variant | A/G;T | snv | 4 | |||||
rs10211524 | 2 | 64980940 | intron variant | G/A | snv | 0.51 | 4 | ||||
rs1912826 | 4 | 186228386 | intron variant | G/A;C | snv | 4 | |||||
rs2657880 | 12 | 56469986 | 3 prime UTR variant | G/C | snv | 0.15 | 4 | ||||
rs4149310 | 9 | 104826853 | intron variant | A/T | snv | 0.34 | 3 | ||||
rs4788815 | 16 | 71600908 | intergenic variant | A/T | snv | 0.69 | 3 | ||||
rs10511701 | 9 | 22112600 | intron variant | T/A;C | snv | 2 | |||||
rs1333043 | 9 | 22106732 | intron variant | T/A | snv | 0.64 | 2 | ||||
rs16850360 | 4 | 74006728 | intron variant | A/G | snv | 4.2E-02 | 2 | ||||
rs16939881 | 15 | 58179780 | intron variant | G/C;T | snv | 2 | |||||
rs3798722 | 6 | 11040190 | intron variant | A/G | snv | 0.39 | 2 | ||||
rs712964 | 22 | 19168604 | upstream gene variant | T/C | snv | 0.66 | 2 | ||||
rs7341786 | 9 | 22112242 | intron variant | A/C | snv | 0.65 | 2 | ||||
rs7859362 | 9 | 22105928 | intron variant | T/C | snv | 0.64 | 2 | ||||
rs10500569 | 16 | 72722202 | intron variant | G/A;C;T | snv | 1 | |||||
rs10502575 | 18 | 31756628 | downstream gene variant | A/G | snv | 6.9E-02 | 1 | ||||
rs10807323 | 6 | 12794799 | intron variant | G/A | snv | 0.34 | 1 | ||||
rs12051548 | 17 | 4779740 | intron variant | G/C | snv | 7.5E-02 | 1 | ||||
rs12507628 | 4 | 72779634 | regulatory region variant | G/A | snv | 0.13 | 1 | ||||
rs1333050 | 9 | 22125914 | intron variant | C/T | snv | 0.50 | 1 | ||||
rs1537371 | 9 | 22099569 | intron variant | C/A;T | snv | 1 | |||||
rs1556516 | 9 | 22100177 | intron variant | G/A;C | snv | 1 |