Source: GWASCAT
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11220463 | 11 | 126378316 | intron variant | A/T | snv | 0.12 | 3 | ||||
rs68055275 | 11 | 126369248 | intron variant | -/T;TT | delins | 3 | |||||
rs76970536 | 11 | 126380785 | intron variant | G/A;T | snv | 3 | |||||
rs10893499 | 11 | 126372084 | intron variant | G/A | snv | 0.16 | 2 | ||||
rs11220462 | 11 | 126374057 | intron variant | G/A | snv | 0.12 | 2 | ||||
rs4307732 | 11 | 126375060 | non coding transcript exon variant | G/A | snv | 0.13 | 2 | ||||
rs59379014 | 11 | 126358105 | intron variant | C/T | snv | 0.12 | 2 |