Source: CURATED
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs9274299 | 1.000 | 0.040 | 6 | 32664181 | non coding transcript exon variant | C/A;G;T | snv | 1.7E-03 | 2 | ||
rs9274390 | 0.925 | 0.080 | 6 | 32664882 | missense variant | C/G;T | snv | 3.9E-02 | 2 | ||
rs9274657 | 1.000 | 0.040 | 6 | 32668587 | upstream gene variant | G/A | snv | 0.37 | 2 | ||
rs77296290 | 1.000 | 0.040 | 6 | 32667519 | intron variant | C/T | snv | 1 | |||
rs9274623 | 1.000 | 0.040 | 6 | 32668221 | intron variant | G/C;T | snv | 1 |