Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7922612 | 0.752 | 0.080 | 10 | 94051682 | intron variant | C/T | snv | 0.39 | 14 | ||
rs10484761 | 0.807 | 0.080 | 6 | 40834522 | intergenic variant | T/C | snv | 0.31 | 7 | ||
rs2274224 | 0.882 | 0.080 | 10 | 94279840 | missense variant | G/A;C | snv | 8.8E-05; 0.44 | 6 | ||
rs10509670 | 0.851 | 0.080 | 10 | 94308190 | intron variant | A/G | snv | 0.30 | 5 | ||
rs13016963 | 0.851 | 0.080 | 2 | 201298088 | intron variant | A/G | snv | 0.59 | 5 | ||
rs2014300 | 0.851 | 0.080 | 21 | 34985564 | intron variant | A/G;T | snv | 0.75 | 5 | ||
rs2228059 | 0.882 | 0.080 | 10 | 5960405 | missense variant | T/G | snv | 0.51 | 0.55 | 5 | |
rs4462560 | 0.851 | 0.080 | 15 | 75355623 | 3 prime UTR variant | G/C | snv | 0.64 | 5 | ||
rs756826500 | 0.925 | 0.080 | 19 | 45413705 | missense variant | G/A | snv | 4.0E-06 | 5 | ||
rs11473 | 0.882 | 0.080 | 19 | 582982 | 3 prime UTR variant | C/A;T | snv | 4 | |||
rs11548103 | 0.882 | 0.080 | 1 | 153615864 | splice region variant | C/T | snv | 0.40 | 0.39 | 4 | |
rs145188037 | 0.925 | 0.080 | 7 | 45914866 | missense variant | G/A | snv | 1.1E-02 | 9.9E-03 | 4 | |
rs1595066 | 0.882 | 0.080 | 2 | 211377000 | 3 prime UTR variant | C/T | snv | 0.28 | 4 | ||
rs16845990 | 0.882 | 0.080 | 2 | 211378286 | 3 prime UTR variant | T/A;C | snv | 4 | |||
rs2244438 | 0.882 | 0.080 | 2 | 201387816 | missense variant | G/A;T | snv | 0.29; 4.0E-06 | 4 | ||
rs353163 | 0.882 | 0.080 | 4 | 67919056 | missense variant | T/A;C;G | snv | 0.67 | 4 | ||
rs3738894 | 0.882 | 0.080 | 2 | 46187030 | 3 prime UTR variant | G/A | snv | 1.1E-02 | 4 | ||
rs1014867 | 0.925 | 0.080 | 4 | 125491736 | missense variant | C/T | snv | 4.9E-02 | 4.9E-02 | 3 | |
rs1039808 | 0.925 | 0.080 | 4 | 125318831 | missense variant | C/G;T | snv | 4.0E-06; 0.41 | 3 | ||
rs12508222 | 0.925 | 0.080 | 4 | 125449492 | missense variant | G/A;T | snv | 4.3E-02; 2.0E-05 | 3 | ||
rs1364898025 | 0.925 | 0.080 | 11 | 108227656 | missense variant | G/A | snv | 3 | |||
rs1567047 | 0.925 | 0.080 | 4 | 125451587 | missense variant | G/A | snv | 0.27 | 0.22 | 3 | |
rs2320615 | 0.925 | 0.080 | 4 | 163148797 | intron variant | A/G | snv | 0.78 | 3 | ||
rs312986 | 0.925 | 0.080 | 18 | 1898710 | intron variant | A/G;T | snv | 3 | |||
rs31564 | 0.925 | 0.080 | 5 | 135894564 | intron variant | G/A;T | snv | 3 |