Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4680 | 0.442 | 0.920 | 22 | 19963748 | missense variant | G/A | snv | 0.46 | 0.44 | 249 | |
rs25531 | 0.581 | 0.520 | 17 | 30237328 | upstream gene variant | T/C | snv | 0.18 | 72 | ||
rs16969968 | 0.653 | 0.360 | 15 | 78590583 | missense variant | G/A | snv | 0.26 | 0.24 | 37 | |
rs1611115 | 0.732 | 0.280 | 9 | 133635393 | upstream gene variant | T/C | snv | 0.80 | 16 | ||
rs1042114 | 0.807 | 0.120 | 1 | 28812463 | missense variant | G/C;T | snv | 0.91 | 6 | ||
rs1079597 | 0.827 | 0.080 | 11 | 113425564 | intron variant | C/T | snv | 0.18 | 5 | ||
rs1126671 | 0.851 | 0.120 | 4 | 99127263 | missense variant | T/C | snv | 0.76 | 0.75 | 5 | |
rs2234918 | 0.827 | 0.200 | 1 | 28863085 | synonymous variant | C/T | snv | 0.59 | 0.50 | 5 | |
rs1042363 | 0.882 | 0.080 | 6 | 151356693 | 3 prime UTR variant | T/C | snv | 4 | |||
rs2952621 | 0.882 | 0.080 | 2 | 129240870 | downstream gene variant | T/A;C | snv | 4 | |||
rs149775276 | 0.925 | 0.080 | 8 | 42732292 | missense variant | C/T | snv | 3.6E-04 | 4.9E-04 | 2 | |
rs779838446 | 0.925 | 0.080 | 8 | 42756217 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 2 |