Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1136905 | 0.882 | 0.120 | 6 | 32518660 | missense variant | T/A;C | snv | 4.2E-03 | 3 | ||
rs11683487 | 0.882 | 0.120 | 2 | 151286035 | intron variant | G/T | snv | 0.36 | 3 | ||
rs121964872 | 0.882 | 0.120 | 16 | 68833362 | missense variant | A/G | snv | 4.4E-05 | 1.1E-04 | 3 | |
rs13063604 | 0.882 | 0.120 | 3 | 128085887 | intron variant | G/A | snv | 0.23 | 3 | ||
rs147961867 | 0.882 | 0.120 | 16 | 30121998 | missense variant | T/C | snv | 5.6E-05 | 2.8E-05 | 3 | |
rs1516982 | 0.882 | 0.120 | 8 | 128521400 | intron variant | A/G | snv | 0.16 | 3 | ||
rs1649942 | 0.925 | 0.120 | 10 | 82191935 | intron variant | G/A;C | snv | 3 | |||
rs1805129 | 0.882 | 0.120 | 22 | 28734470 | synonymous variant | T/C | snv | 3.6E-02 | 4.0E-02 | 3 | |
rs186724 | 0.882 | 0.120 | 1 | 110018293 | intron variant | C/G;T | snv | 3 | |||
rs2191249 | 0.882 | 0.120 | 17 | 61758503 | intron variant | T/G | snv | 0.79 | 3 | ||
rs2228026 | 0.882 | 0.120 | 14 | 20395890 | synonymous variant | A/G | snv | 4.7E-02 | 3.8E-02 | 3 | |
rs2252673 | 0.882 | 0.120 | 19 | 7150407 | intron variant | C/G | snv | 0.75 | 3 | ||
rs2287497 | 0.882 | 0.120 | 17 | 7689462 | intron variant | G/A | snv | 0.25 | 3 | ||
rs266851 | 0.882 | 0.120 | 19 | 50833083 | intron variant | C/T | snv | 0.20 | 3 | ||
rs34529039 | 0.882 | 0.120 | 19 | 33301725 | synonymous variant | C/A | snv | 0.19 | 0.16 | 3 | |
rs35068177 | 0.882 | 0.120 | 7 | 87550213 | synonymous variant | T/C | snv | 2.2E-04 | 3.1E-04 | 3 | |
rs351771 | 0.882 | 0.120 | 5 | 112828864 | synonymous variant | G/A | snv | 0.65 | 0.59 | 3 | |
rs3976507 | 0.882 | 0.120 | 3 | 179239995 | 3 prime UTR variant | C/T | snv | 0.19 | 0.24 | 3 | |
rs4320932 | 0.882 | 0.120 | 11 | 2150371 | intron variant | T/C | snv | 0.19 | 3 | ||
rs4648551 | 0.882 | 0.120 | 1 | 3716166 | intron variant | G/A | snv | 0.32 | 3 | ||
rs4954956 | 0.882 | 0.120 | 2 | 138787007 | regulatory region variant | C/T | snv | 0.25 | 3 | ||
rs55854959 | 0.882 | 0.120 | 13 | 32330979 | missense variant | G/A | snv | 2.4E-05 | 1.4E-04 | 3 | |
rs56318008 | 0.925 | 0.120 | 1 | 22143914 | 5 prime UTR variant | C/T | snv | 0.13 | 3 | ||
rs567534295 | 0.882 | 0.120 | 17 | 43048090 | intron variant | C/T | snv | 2.8E-05 | 3 | ||
rs587780191 | 0.882 | 0.120 | 22 | 28699931 | missense variant | T/C;G | snv | 4.0E-06; 1.6E-05 | 3 |