Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1231813088 | 0.851 | 0.160 | 10 | 92690015 | missense variant | C/T | snv | 4 | |||
rs1322425552 | 0.851 | 0.160 | 17 | 74923048 | missense variant | G/A | snv | 4 | |||
rs137852959 | 0.790 | 0.160 | 20 | 3918695 | missense variant | G/A | snv | 8.7E-05 | 2.3E-04 | 9 | |
rs145522851 | 0.925 | 0.080 | 11 | 66685935 | missense variant | C/T | snv | 1.0E-04 | 1.2E-04 | 4 | |
rs3755557 | 0.807 | 0.280 | 3 | 120096110 | non coding transcript exon variant | T/A | snv | 0.14 | 6 | ||
rs6280 | 0.602 | 0.520 | 3 | 114171968 | missense variant | C/T | snv | 0.63 | 0.54 | 57 | |
rs6313 | 0.562 | 0.640 | 13 | 46895805 | synonymous variant | G/A | snv | 0.41 | 0.40 | 82 | |
rs6779828 | 0.925 | 0.120 | 3 | 120056300 | intron variant | C/T | snv | 0.28 | 2 | ||
rs945232586 | 1.000 | 0.080 | 19 | 15641443 | missense variant | G/A | snv | 1 | |||
rs953038635 | 0.590 | 0.800 | 6 | 159692720 | missense variant | G/A;T | snv | 8.0E-06 | 51 |