Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2076530 | 0.724 | 0.640 | 6 | 32396039 | missense variant | T/C | snv | 0.42 | 0.40 | 5 | |
rs2395182 | 0.851 | 0.280 | 6 | 32445540 | downstream gene variant | G/T | snv | 0.76 | 5 | ||
rs3817963 | 0.776 | 0.360 | 6 | 32400310 | intron variant | T/C | snv | 0.25 | 5 | ||
rs615672 | 0.851 | 0.240 | 6 | 32606394 | intergenic variant | G/A;C | snv | 5 | |||
rs7194 | 0.827 | 0.280 | 6 | 32444703 | 3 prime UTR variant | G/A | snv | 0.61 | 5 | ||
rs3129768 | 0.851 | 0.240 | 6 | 32627306 | upstream gene variant | G/T | snv | 0.76 | 4 | ||
rs9268402 | 0.827 | 0.200 | 6 | 32373576 | intron variant | G/A | snv | 0.45 | 4 | ||
rs3763307 | 0.882 | 0.200 | 6 | 32406845 | non coding transcript exon variant | A/T | snv | 0.24 | 3 | ||
rs9268403 | 0.807 | 0.240 | 6 | 32373696 | intron variant | T/C | snv | 0.24 | 3 | ||
rs9268480 | 0.882 | 0.200 | 6 | 32396067 | synonymous variant | C/T | snv | 0.26 | 0.24 | 3 | |
rs9271640 | 0.925 | 0.120 | 6 | 32624423 | upstream gene variant | T/C | snv | 0.76 | 2 |