Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs73036519 | 0.851 | 0.040 | 19 | 45245104 | intron variant | G/A;C | snv | 5 | |||
rs3138141 | 0.827 | 0.040 | 12 | 55721994 | 3 prime UTR variant | C/A | snv | 0.19 | 0.16 | 5 | |
rs11755724 | 0.807 | 0.320 | 6 | 7118757 | intron variant | A/G;T | snv | 5 | |||
rs11080055 | 0.851 | 0.040 | 17 | 28322698 | intron variant | A/C | snv | 0.54 | 5 | ||
rs10781182 | 0.851 | 0.040 | 9 | 74002804 | intergenic variant | T/G | snv | 0.54 | 4 | ||
rs114092250 | 0.851 | 0.040 | 5 | 35494346 | intergenic variant | G/A;T | snv | 4 | |||
rs142450006 | 0.851 | 0.040 | 20 | 45986353 | regulatory region variant | TTCT/-;TTCTTTCT | delins | 2.0E-02 | 4 | ||
rs148553336 | 0.851 | 0.040 | 1 | 196644043 | intergenic variant | T/C | snv | 7.7E-03 | 4 | ||
rs1626340 | 0.827 | 0.120 | 9 | 99161090 | intergenic variant | G/A;T | snv | 4 | |||
rs201459901 | 0.851 | 0.040 | 20 | 58078668 | regulatory region variant | -/A | delins | 0.21 | 4 | ||
rs61818925 | 0.851 | 0.040 | 1 | 196846320 | upstream gene variant | T/G | snv | 0.67 | 4 | ||
rs61941274 | 0.827 | 0.160 | 12 | 111694806 | intron variant | G/A;T | snv | 4 | |||
rs62247658 | 0.851 | 0.040 | 3 | 64729479 | intron variant | C/T | snv | 0.42 | 4 | ||
rs1800625 | 0.641 | 0.680 | 6 | 32184665 | upstream gene variant | A/G | snv | 0.15 | 4 | ||
rs12357257 | 0.851 | 0.040 | 10 | 24710664 | intron variant | G/A | snv | 0.18 | 4 | ||
rs10490924 | 0.716 | 0.240 | 10 | 122454932 | missense variant | G/T | snv | 0.26 | 0.23 | 4 | |
rs3750846 | 0.851 | 0.040 | 10 | 122456049 | intron variant | T/C | snv | 0.24 | 4 | ||
rs9564692 | 0.851 | 0.040 | 13 | 31247103 | splice region variant | C/T | snv | 0.40 | 0.36 | 4 | |
rs147859257 | 0.827 | 0.040 | 19 | 6718135 | missense variant | T/G | snv | 2.8E-03 | 2.4E-03 | 4 | |
rs2230199 | 0.763 | 0.240 | 19 | 6718376 | missense variant | G/C;T | snv | 0.15 | 4 | ||
rs1864163 | 0.882 | 0.120 | 16 | 56963321 | intron variant | G/A | snv | 0.26 | 4 | ||
rs2303790 | 0.724 | 0.280 | 16 | 56983380 | missense variant | A/G | snv | 2.6E-03 | 6.5E-04 | 4 | |
rs5817082 | 0.851 | 0.040 | 16 | 56963437 | intron variant | -/A | delins | 4 | |||
rs641153 | 0.790 | 0.160 | 6 | 31946403 | missense variant | G/A;T | snv | 9.6E-02; 4.1E-06 | 4 | ||
rs121913059 | 0.716 | 0.280 | 1 | 196747245 | missense variant | C/T | snv | 1.4E-04 | 1.9E-04 | 4 |