Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11204896 | 1 | 151824266 | intron variant | C/G | snv | 7.6E-02 | 1 | ||||
rs11217036 | 11 | 118805063 | intergenic variant | C/G;T | snv | 1 | |||||
rs11236814 | 11 | 76632384 | upstream gene variant | A/T | snv | 0.13 | 1 | ||||
rs11255968 | 10 | 8894199 | upstream gene variant | C/T | snv | 9.3E-02 | 1 | ||||
rs11464691 | 17 | 40614389 | intergenic variant | -/A | delins | 0.68 | 1 | ||||
rs1147169 | 2 | 198036671 | intron variant | T/C | snv | 0.67 | 1 | ||||
rs11652139 | 17 | 39992780 | intron variant | G/A;C | snv | 1 | |||||
rs11727978 | 4 | 38809430 | intron variant | T/A | snv | 0.14 | 1 | ||||
rs12045923 | 1 | 10583772 | intron variant | C/G;T | snv | 1 | |||||
rs12551834 | 9 | 128850912 | intron variant | G/A | snv | 7.4E-02 | 1 | ||||
rs12596613 | 16 | 11397150 | intron variant | C/G | snv | 0.29 | 1 | ||||
rs13088318 | 3 | 101523907 | downstream gene variant | A/G;T | snv | 0.24 | 1 | ||||
rs13153019 | 5 | 177355217 | upstream gene variant | T/C | snv | 0.21 | 1 | ||||
rs13384448 | 2 | 227843146 | intergenic variant | C/T | snv | 0.67 | 1 | ||||
rs13403656 | 2 | 111511550 | intron variant | A/T | snv | 0.84 | 1 | ||||
rs1444789 | 10 | 9022398 | intergenic variant | T/C | snv | 0.23 | 1 | ||||
rs150254607 | 4 | 122532955 | intergenic variant | -/TAT | ins | 4.9E-02 | 1 | ||||
rs1505992 | 5 | 40498475 | intron variant | A/T | snv | 0.61 | 1 | ||||
rs16899524 | 6 | 31394533 | non coding transcript exon variant | C/T | snv | 0.10 | 1 | ||||
rs16922576 | 9 | 5064193 | intron variant | T/C | snv | 0.25 | 1 | ||||
rs17607589 | 3 | 188684798 | intron variant | C/T | snv | 0.13 | 1 | ||||
rs17664743 | 7 | 50214301 | intron variant | G/A | snv | 0.24 | 1 | ||||
rs1775550 | 10 | 9010779 | regulatory region variant | G/A;C | snv | 1 | |||||
rs1814576 | 5 | 110824180 | intergenic variant | T/C | snv | 7.0E-02 | 1 | ||||
rs1997502 | 2 | 102227789 | intron variant | A/G;T | snv | 1 |