Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs370911 | 1 | 162323515 | intron variant | A/G | snv | 0.99 | 6 | ||||
rs4251583 | 12 | 43783705 | missense variant | A/G | snv | 8.6E-04 | 1.1E-03 | 6 | |||
rs5176 | 1 | 53246137 | 3 prime UTR variant | T/G | snv | 6.4E-04 | 6 | ||||
rs533617 | 2 | 21011100 | missense variant | T/C | snv | 3.1E-02 | 2.9E-02 | 6 | |||
rs583104 | 1 | 109278685 | downstream gene variant | G/T | snv | 0.63 | 6 | ||||
rs660240 | 1 | 109275216 | 3 prime UTR variant | T/C | snv | 0.75 | 6 | ||||
rs737410 | 11 | 75315038 | intron variant | A/G | snv | 4.3E-02 | 6 | ||||
rs760242 | 11 | 71435530 | missense variant | C/T | snv | 2.2E-04 | 6.3E-05 | 6 | |||
rs7993724 | 13 | 27919139 | upstream gene variant | T/C | snv | 5.6E-03 | 6 | ||||
rs8138057 | 22 | 37665537 | intron variant | G/A | snv | 3.0E-03 | 1.3E-02 | 6 | |||
rs9341023 | 6 | 152062578 | intron variant | C/T | snv | 6 | |||||
rs9622186 | 22 | 35377961 | upstream gene variant | A/G | snv | 3.7E-03 | 6 | ||||
rs10199768 | 2 | 21021128 | intron variant | G/T | snv | 0.35 | 5 | ||||
rs10478730 | 6 | 12297276 | downstream gene variant | C/T | snv | 1.2E-02 | 5 | ||||
rs1065853 | 19 | 44909976 | non coding transcript exon variant | G/A;C;T | snv | 5 | |||||
rs10789117 | 1 | 62606594 | intron variant | A/C;T | snv | 5 | |||||
rs11563251 | 2 | 233770738 | 3 prime UTR variant | C/T | snv | 0.19 | 5 | ||||
rs11828157 | 11 | 102947395 | intron variant | G/A | snv | 4.7E-02 | 5 | ||||
rs11921179 | 3 | 129976195 | intron variant | G/A | snv | 0.96 | 5 | ||||
rs1321655 | 1 | 160124668 | intron variant | A/G;T | snv | 5 | |||||
rs1456649 | 1 | 240288305 | intron variant | G/C | snv | 3.0E-03 | 5 | ||||
rs16880248 | 6 | 88141968 | 3 prime UTR variant | G/T | snv | 2.7E-02 | 5 | ||||
rs17243641 | 9 | 136886986 | intron variant | G/T | snv | 2.6E-03 | 5 | ||||
rs17404153 | 3 | 132444356 | intron variant | G/T | snv | 0.10 | 5 | ||||
rs1748197 | 1 | 62590441 | intron variant | G/A | snv | 0.42 | 5 |