Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1800871 | 0.508 | 0.800 | 1 | 206773289 | 5 prime UTR variant | A/G | snv | 0.69 | 108 | ||
rs909253 | 0.641 | 0.600 | 6 | 31572536 | intron variant | A/G;T | snv | 34 | |||
rs10484554 | 0.807 | 0.200 | 6 | 31306778 | intron variant | C/T | snv | 0.12 | 11 | ||
rs2248462 | 0.807 | 0.240 | 6 | 31479019 | downstream gene variant | G/A | snv | 0.19 | 10 | ||
rs2844511 | 0.807 | 0.200 | 6 | 31422007 | intron variant | A/G;T | snv | 10 | |||
rs3130380 | 0.807 | 0.280 | 6 | 30311353 | intron variant | G/A | snv | 6.6E-02 | 10 | ||
rs12198173 | 0.827 | 0.240 | 6 | 32059031 | intron variant | G/A | snv | 0.10 | 9 | ||
rs3093662 | 0.851 | 0.200 | 6 | 31576412 | intron variant | A/G | snv | 7.1E-02 | 9 | ||
rs2894207 | 0.882 | 0.160 | 6 | 31295974 | intron variant | T/C | snv | 0.20 | 8 | ||
rs3815087 | 0.851 | 0.200 | 6 | 31125810 | 5 prime UTR variant | G/A | snv | 0.25 | 8 | ||
rs3823418 | 0.925 | 0.120 | 6 | 31133165 | intron variant | G/A | snv | 0.23 | 8 | ||
rs4324798 | 0.790 | 0.240 | 6 | 28808340 | intergenic variant | G/A | snv | 7.2E-02 | 8 | ||
rs9368699 | 0.851 | 0.200 | 6 | 31834764 | non coding transcript exon variant | T/C | snv | 3.2E-02 | 8 | ||
rs2516509 | 0.882 | 0.160 | 6 | 31482217 | intron variant | T/C | snv | 0.19 | 7 | ||
rs1235162 | 0.827 | 0.280 | 6 | 29569447 | intron variant | A/G | snv | 6.0E-02 | 6 | ||
rs2284178 | 0.925 | 0.120 | 6 | 31464348 | non coding transcript exon variant | C/T | snv | 0.44 | 6 | ||
rs2844513 | 0.925 | 0.120 | 6 | 31420437 | intron variant | G/A | snv | 0.53 | 6 | ||
rs527476195 | 0.925 | 0.120 | 6 | 31133165 | intron variant | G/A | snv | 6 | |||
rs7756521 | 1.000 | 6 | 30880476 | intron variant | T/C | snv | 0.25 | 5 | |||
rs3117143 | 0.882 | 0.160 | 6 | 29063365 | intron variant | C/A | snv | 5.2E-02 | 4 | ||
rs1233579 | 0.925 | 0.160 | 6 | 28744886 | intergenic variant | A/G | snv | 7.2E-02 | 3 | ||
rs13194504 | 0.925 | 0.120 | 6 | 28662914 | intergenic variant | G/A | snv | 5.1E-02 | 3 | ||
rs3131093 | 0.925 | 0.160 | 6 | 28869660 | intergenic variant | C/T | snv | 7.1E-02 | 3 | ||
rs11884476 | 2 | 205453869 | intron variant | C/G | snv | 0.11 | 1 | ||||
rs4118325 | 1 | 107035210 | intergenic variant | G/A;T | snv | 1 |