Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs671 | 0.593 | 0.464 | 12 | 111803962 | missense variant | G/A | snp | 1.9E-02 | 1.3E-02 | 23 | |
rs886424 | 0.744 | 0.250 | 6 | 30814225 | non coding transcript exon variant | C/T | snp | 7.1E-02 | 9.1E-02 | 16 | |
rs13107325 | 1.000 | 0.036 | 4 | 102267552 | missense variant | C/A,T | snp | 4.0E-06; 4.5E-02 | 4.3E-02 | 14 | |
rs1006737 | 0.679 | 0.107 | 12 | 2236129 | intron variant | G/A | snp | 0.37 | 13 | ||
rs7903146 | 0.596 | 0.536 | 10 | 112998590 | intron variant | C/G,T | snp | 0.26 | 13 | ||
rs8321 | 0.734 | 0.250 | 6 | 30064745 | 3 prime UTR variant | A/C | snp | 5.4E-02 | 6.5E-02 | 13 | |
rs3129817 | 0.724 | 0.286 | 6 | 30374976 | intergenic variant | G/A | snp | 0.12 | 12 | ||
rs2524005 | 0.821 | 0.036 | 6 | 29931900 | intron variant | G/A | snp | 0.17 | 11 | ||
rs4650608 | 0.801 | 0.036 | 1 | 78772330 | intergenic variant | T/C | snp | 0.31 | 11 | ||
rs10275045 | 0.801 | 0.143 | 7 | 1881190 | intron variant | C/T | snp | 0.33 | 11 | ||
rs1480380 | 0.744 | 0.321 | 6 | 32945469 | intron variant | C/T | snp | 0.11 | 10 | ||
rs17693963 | 0.821 | 0.036 | 6 | 27742386 | intergenic variant | A/C,G | snp | 6.4E-02 | 10 | ||
rs17746001 | 0.821 | 0.036 | 4 | 179734472 | intergenic variant | C/T | snp | 4.4E-02 | 10 | ||
rs9834970 | 0.821 | 0.036 | 3 | 36814539 | intergenic variant | T/C | snp | 0.44 | 10 | ||
rs4356203 | 0.821 | 0.036 | 11 | 17138601 | intron variant | A/G | snp | 0.33 | 10 | ||
rs7872515 | 0.821 | 0.036 | 9 | 92060258 | intron variant | G/A | snp | 0.24 | 10 | ||
rs7219021 | 0.821 | 0.036 | 17 | 48763179 | intron variant | T/G | snp | 0.24 | 10 | ||
rs4949526 | 0.846 | 0.036 | 1 | 29959372 | intergenic variant | T/C | snp | 0.56 | 9 | ||
rs12201676 | 0.821 | 0.036 | 6 | 89022382 | intergenic variant | T/C | snp | 0.21 | 8 | ||
rs3782886 | 0.784 | 0.250 | 12 | 111672685 | synonymous variant | T/C | snp | 1.9E-02 | 1.4E-02 | 8 | |
rs802568 | 0.821 | 0.036 | 7 | 146262151 | intron variant | T/G | snp | 0.16 | 8 | ||
rs11789399 | 0.801 | 0.036 | 9 | 118597008 | intergenic variant | G/A,C | snp | 0.35 | 8 | ||
rs11191580 | 0.821 | 0.036 | 10 | 103146454 | intron variant | T/C | snp | 8.2E-02 | 8 | ||
rs17782313 | 0.734 | 0.250 | 18 | 60183864 | intergenic variant | T/C | snp | 0.23 | 7 | ||
rs9275524 | 0.784 | 0.143 | 6 | 32707332 | intergenic variant | T/C | snp | 0.57 | 7 |