Source: GWASCAT ×
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1047891 | 0.827 | 0.200 | 2 | 210675783 | missense variant | C/A | snv | 0.30 | 0.33 | 25 | |
rs1799945 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 16 | |
rs13331259 | 16 | 249924 | intron variant | A/G | snv | 3.0E-02 | 14 | ||||
rs7776054 | 6 | 135097778 | intron variant | A/G | snv | 0.24 | 13 | ||||
rs2736100 | 0.550 | 0.880 | 5 | 1286401 | 3 prime UTR variant | C/A | snv | 0.52 | 12 | ||
rs3811444 | 1 | 247876149 | missense variant | C/T | snv | 0.31 | 0.26 | 12 | |||
rs7775698 | 1.000 | 0.080 | 6 | 135097497 | intron variant | C/T | snv | 6.9E-02 | 11 | ||
rs17758695 | 18 | 63253621 | intron variant | C/T | snv | 2.1E-02 | 10 | ||||
rs2283847 | 22 | 27785411 | intron variant | C/A;G;T | snv | 7 | |||||
rs9399137 | 0.851 | 0.320 | 6 | 135097880 | intron variant | T/C | snv | 0.20 | 6 | ||
rs78909033 | 2 | 240571486 | intron variant | G/A | snv | 9.2E-02 | 5 | ||||
rs149290349 | 2 | 43224818 | missense variant | G/A;T | snv | 6.7E-02 | 3 | ||||
rs1555405 | 14 | 100710432 | regulatory region variant | G/A | snv | 0.29 | 2 |