Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs185819 | 0.851 | 0.200 | 6 | 32082290 | missense variant | T/A;C;G | snv | 8.2E-06; 0.58; 4.1E-06 | 8 | ||
rs1150754 | 0.851 | 0.200 | 6 | 32082981 | intron variant | C/A;T | snv | 2 | |||
rs1150753 | 0.925 | 0.120 | 6 | 32092090 | intron variant | A/G | snv | 6.3E-02 | 1 | ||
rs2269426 | 0.807 | 0.280 | 6 | 32108722 | intron variant | G/A | snv | 0.35 | 8 | ||
rs3130342 | 1.000 | 0.080 | 6 | 32112369 | non coding transcript exon variant | A/C;G;T | snv | 1 | |||
rs8283 | 0.882 | 0.120 | 6 | 32115523 | 3 prime UTR variant | A/G | snv | 0.25 | 4 |