Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12153855 | 0.776 | 0.320 | 6 | 32107027 | intron variant | T/C | snv | 0.11 | 10 | ||
rs12198173 | 0.827 | 0.240 | 6 | 32059031 | intron variant | G/A | snv | 0.10 | 9 | ||
rs13199524 | 0.807 | 0.240 | 6 | 32098988 | intron variant | C/T | snv | 8.4E-02 | 8 | ||
rs185819 | 0.851 | 0.200 | 6 | 32082290 | missense variant | T/A;C;G | snv | 8.2E-06; 0.58; 4.1E-06 | 8 | ||
rs2269426 | 0.807 | 0.280 | 6 | 32108722 | intron variant | G/A | snv | 0.35 | 8 | ||
rs1150752 | 0.882 | 0.240 | 6 | 32096949 | missense variant | T/C;G | snv | 5.9E-02 | 3 | ||
rs3134954 | 0.882 | 0.240 | 6 | 32104116 | intron variant | C/T | snv | 0.90 | 3 | ||
rs1150754 | 0.851 | 0.200 | 6 | 32082981 | intron variant | C/A;T | snv | 2 |