Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12916 | 0.807 | 0.240 | 5 | 75360714 | 3 prime UTR variant | T/C;G | snv | 0.37 | 12 | ||
rs12654264 | 0.925 | 0.120 | 5 | 75352778 | intron variant | A/T | snv | 0.38 | 7 | ||
rs3846663 | 0.882 | 0.120 | 5 | 75359901 | intron variant | C/T | snv | 0.35 | 7 | ||
rs17238484 | 1.000 | 0.080 | 5 | 75352671 | intron variant | G/T | snv | 0.22 | 4 | ||
rs3761740 | 0.882 | 0.160 | 5 | 75336308 | intron variant | C/A | snv | 8.2E-02 | 4 | ||
rs10038095 | 5 | 75341886 | intron variant | A/T | snv | 0.38 | 3 | ||||
rs10474434 | 5 | 75348856 | intron variant | G/T | snv | 0.20 | 3 | ||||
rs3761739 | 5 | 75335676 | intron variant | C/T | snv | 0.15 | 3 | ||||
rs6453131 | 5 | 75348881 | intron variant | T/G | snv | 0.39 | 3 | ||||
rs10045497 | 5 | 75340659 | intron variant | C/A | snv | 0.35 | 2 | ||||
rs17238540 | 1.000 | 0.040 | 5 | 75359673 | non coding transcript exon variant | T/G | snv | 4.0E-02 | 2 | ||
rs3843482 | 5 | 75343434 | intron variant | T/G | snv | 0.35 | 2 | ||||
rs4629571 | 0.925 | 0.160 | 5 | 75362479 | intron variant | A/G | snv | 8.7E-02 | 2 | ||
rs3846661 | 5 | 75343353 | intron variant | A/G | snv | 0.56 | 1 | ||||
rs3846662 | 0.763 | 0.280 | 5 | 75355259 | non coding transcript exon variant | A/G | snv | 0.50 | 0.58 | 12 |