Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6937121 | 6 | 142385996 | intron variant | T/G | snv | 0.47 | 2 | ||||
rs7753012 | 6 | 142424746 | intron variant | T/G | snv | 0.50 | 2 | ||||
rs972982 | 6 | 142345724 | intron variant | T/C | snv | 0.44 | 2 | ||||
rs3748069 | 6 | 142446496 | downstream gene variant | A/G | snv | 0.39 | 3 | ||||
rs4896582 | 6 | 142382740 | intron variant | G/A | snv | 0.50 | 3 | ||||
rs7741741 | 0.925 | 0.040 | 6 | 142334664 | intron variant | T/A;G | snv | 3 | |||
rs6570507 | 0.827 | 0.240 | 6 | 142358435 | intron variant | G/A | snv | 0.47 | 6 |