Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs340874 | 0.882 | 0.080 | 1 | 213985913 | non coding transcript exon variant | T/C | snv | 0.40 | 7 | ||
rs17712208 | 1 | 213977102 | intron variant | T/A | snv | 2.1E-02 | 2 | ||||
rs340878 | 1 | 213983706 | intron variant | G/C | snv | 0.63 | 2 | ||||
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 81 | |
rs780094 | 0.658 | 0.400 | 2 | 27518370 | intron variant | T/C | snv | 0.67 | 62 | ||
rs560887 | 0.827 | 0.120 | 2 | 168906638 | intron variant | T/C | snv | 0.79 | 0.80 | 18 | |
rs2068834 | 0.925 | 0.120 | 2 | 27616672 | intron variant | T/C | snv | 0.28 | 10 | ||
rs13023194 | 0.925 | 0.120 | 2 | 27744393 | intergenic variant | G/A;C | snv | 4 | |||
rs13404446 | 0.925 | 0.120 | 2 | 27296386 | intron variant | G/A | snv | 0.42 | 4 | ||
rs2305929 | 1.000 | 0.040 | 2 | 27891044 | intron variant | A/G | snv | 0.14 | 4 | ||
rs4665965 | 0.925 | 0.120 | 2 | 27313513 | intron variant | T/A;C | snv | 4 | |||
rs780110 | 0.925 | 0.120 | 2 | 27462521 | intron variant | G/A | snv | 0.56 | 4 | ||
rs853789 | 2 | 168944978 | intron variant | A/G;T | snv | 0.75 | 4 | ||||
rs1371614 | 2 | 26930006 | intron variant | C/T | snv | 0.29 | 3 | ||||
rs1124649 | 2 | 27037601 | missense variant | G/A | snv | 0.32 | 0.35 | 2 | |||
rs11891554 | 2 | 27390750 | intron variant | G/A;T | snv | 7.1E-02 | 2 | ||||
rs2390732 | 2 | 168749457 | intron variant | G/A | snv | 0.65 | 2 | ||||
rs4402960 | 0.724 | 0.400 | 3 | 185793899 | intron variant | G/T | snv | 0.38 | 21 | ||
rs11708067 | 0.882 | 0.080 | 3 | 123346931 | intron variant | A/G | snv | 0.19 | 9 | ||
rs11920090 | 1.000 | 0.040 | 3 | 170999732 | intron variant | T/A | snv | 0.20 | 5 | ||
rs7651090 | 0.925 | 0.080 | 3 | 185795604 | intron variant | A/G | snv | 0.39 | 5 | ||
rs2877716 | 3 | 123375604 | intron variant | T/C | snv | 0.76 | 4 | ||||
rs11717195 | 1.000 | 0.080 | 3 | 123363551 | intron variant | T/C | snv | 0.19 | 3 | ||
rs11715915 | 3 | 49417897 | synonymous variant | C/A;T | snv | 0.28 | 2 | ||||
rs1280 | 3 | 170995501 | intron variant | T/C | snv | 0.20 | 2 |