Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 34 | |
rs12203592 | 0.649 | 0.320 | 6 | 396321 | intron variant | C/T | snv | 0.10 | 20 | ||
rs72928038 | 0.695 | 0.360 | 6 | 90267049 | intron variant | G/A | snv | 0.11 | 19 | ||
rs2111485 | 0.724 | 0.280 | 2 | 162254026 | regulatory region variant | A/G | snv | 0.46 | 12 | ||
rs4409785 | 0.752 | 0.240 | 11 | 95578258 | intron variant | T/C | snv | 0.13 | 12 | ||
rs6059655 | 0.790 | 0.080 | 20 | 34077942 | intron variant | A/G | snv | 0.95 | 10 | ||
rs769449 | 0.882 | 0.120 | 19 | 44906745 | non coding transcript exon variant | G/A | snv | 8.4E-02 | 8 | ||
rs1126809 | 0.683 | 0.320 | 11 | 89284793 | missense variant | G/A | snv | 0.18 | 0.18 | 8 | |
rs71508903 | 0.807 | 0.160 | 10 | 62020112 | intron variant | C/T | snv | 0.15 | 7 | ||
rs1129038 | 0.851 | 0.120 | 15 | 28111713 | 3 prime UTR variant | C/T | snv | 0.49 | 0.50 | 6 | |
rs4986790 | 0.438 | 0.800 | 9 | 117713024 | missense variant | A/G;T | snv | 6.1E-02; 4.0E-06 | 6 | ||
rs10774624 | 0.882 | 0.160 | 12 | 111395984 | intron variant | G/A | snv | 0.67 | 5 | ||
rs1393350 | 0.851 | 0.160 | 11 | 89277878 | intron variant | G/A | snv | 0.17 | 5 | ||
rs251464 | 0.851 | 0.080 | 5 | 149816671 | intron variant | G/C | snv | 0.36 | 5 | ||
rs4766578 | 0.851 | 0.200 | 12 | 111466567 | intron variant | T/A | snv | 0.66 | 4 | ||
rs117744081 | 0.851 | 0.080 | 7 | 29092663 | missense variant | A/G | snv | 2.2E-02 | 2.3E-02 | 4 | |
rs968567 | 0.851 | 0.240 | 11 | 61828092 | intron variant | C/T | snv | 0.11 | 4 | ||
rs2395185 | 0.724 | 0.360 | 6 | 32465390 | intron variant | G/T | snv | 0.29 | 4 | ||
rs10876864 | 0.882 | 0.120 | 12 | 56007301 | upstream gene variant | G/A | snv | 0.50 | 4 | ||
rs706779 | 0.827 | 0.160 | 10 | 6056861 | intron variant | T/C | snv | 0.48 | 4 | ||
rs1801133 | 0.472 | 0.880 | 1 | 11796321 | missense variant | G/A | snv | 0.31 | 0.27 | 4 | |
rs301807 | 0.925 | 0.080 | 1 | 8424763 | intron variant | A/G;T | snv | 4 | |||
rs11203203 | 0.807 | 0.240 | 21 | 42416077 | intron variant | G/A | snv | 0.28 | 4 | ||
rs4268748 | 0.925 | 0.080 | 16 | 89960104 | intron variant | T/C | snv | 0.30 | 3 | ||
rs1701704 | 0.851 | 0.200 | 12 | 56018703 | intron variant | T/G | snv | 0.25 | 3 |