Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10112596 | 0.925 | 0.120 | 8 | 11722293 | intron variant | A/G | snv | 0.83 | 3 | ||
rs2412646 | 0.882 | 0.120 | 4 | 55452605 | 3 prime UTR variant | T/C | snv | 0.58 | 3 | ||
rs463379 | 0.882 | 0.080 | 5 | 1431049 | intron variant | G/C | snv | 0.31 | 3 | ||
rs4964057 | 0.882 | 0.080 | 12 | 27363909 | intron variant | T/G | snv | 0.29 | 3 | ||
rs6350 | 0.882 | 0.080 | 5 | 1443084 | missense variant | G/A;C | snv | 5.6E-02; 6.8E-05 | 3 | ||
rs1015443 | 0.925 | 0.160 | 12 | 10908523 | missense variant | T/A;C | snv | 4.0E-06; 0.59 | 2 | ||
rs11240 | 0.925 | 0.080 | 4 | 55453183 | 3 prime UTR variant | C/A;G | snv | 2 | |||
rs11941860 | 1.000 | 0.080 | 4 | 46080161 | intron variant | C/T | snv | 0.12 | 2 | ||
rs2119183 | 1.000 | 0.080 | 4 | 46270789 | intron variant | G/A | snv | 7.6E-02 | 2 | ||
rs2836016 | 0.925 | 0.080 | 21 | 37840718 | intron variant | G/A | snv | 0.59 | 0.58 | 2 | |
rs3756007 | 1.000 | 0.080 | 4 | 46389047 | 5 prime UTR variant | T/C | snv | 5.4E-02 | 2 | ||
rs3811939 | 1.000 | 0.080 | 5 | 76954762 | intron variant | G/A | snv | 0.27 | 2 | ||
rs536599 | 1.000 | 0.080 | 4 | 46196917 | intergenic variant | G/T | snv | 0.47 | 2 | ||
rs56013859 | 0.925 | 0.080 | 2 | 238276865 | intron variant | T/C | snv | 0.11 | 2 | ||
rs6473797 | 0.925 | 0.080 | 8 | 53240422 | intron variant | T/C | snv | 0.39 | 2 | ||
rs10044881 | 1.000 | 0.080 | 5 | 148645656 | non coding transcript exon variant | T/C | snv | 0.17 | 1 | ||
rs10405681 | 1.000 | 0.080 | 19 | 3634021 | intron variant | C/A;T | snv | 1 | |||
rs10419980 | 1.000 | 0.080 | 19 | 3685118 | intron variant | C/T | snv | 0.29 | 1 | ||
rs10432303 | 1.000 | 0.080 | 19 | 3656654 | intron variant | G/A | snv | 0.41 | 1 | ||
rs11250159 | 1.000 | 0.080 | 8 | 11729725 | intron variant | G/A;T | snv | 1 | |||
rs141973904 | 1.000 | 0.080 | 4 | 99341085 | intron variant | C/T | snv | 1.6E-02 | 1 | ||
rs1476592 | 1.000 | 0.080 | 19 | 3679742 | intron variant | A/G;T | snv | 1 | |||
rs17777298 | 1.000 | 0.080 | 5 | 148541962 | intron variant | T/A | snv | 0.24 | 1 | ||
rs2074957 | 1.000 | 0.080 | 19 | 3653527 | synonymous variant | C/A;T | snv | 8.0E-06; 0.57 | 1 | ||
rs4432372 | 1.000 | 0.080 | 19 | 3698844 | intron variant | A/G;T | snv | 1 |