Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs724577 | 4 | 17991787 | intron variant | A/C | snv | 0.71 | 2 | ||||
rs16896068 | 4 | 17943217 | intron variant | G/A | snv | 0.25 | 1 | ||||
rs2707450 | 4 | 17940937 | intron variant | C/T | snv | 0.73 | 1 | ||||
rs2724475 | 4 | 17944809 | intron variant | T/C | snv | 0.71 | 1 | ||||
rs6830062 | 4 | 18016107 | intron variant | T/C | snv | 0.25 | 1 | ||||
rs6845078 | 4 | 17950585 | intron variant | C/A;T | snv | 1 | |||||
rs7692995 | 4 | 17935011 | intron variant | T/C | snv | 0.23 | 1 | ||||
rs925098 | 4 | 17918188 | intron variant | G/A | snv | 0.70 | 1 |