Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3851179 | 0.752 | 0.280 | 11 | 86157598 | downstream gene variant | T/C | snv | 0.70 | 15 | ||
rs3846662 | 0.763 | 0.280 | 5 | 75355259 | non coding transcript exon variant | A/G | snv | 0.50 | 0.58 | 12 | |
rs2230288 | 0.776 | 0.160 | 1 | 155236376 | missense variant | C/T | snv | 1.0E-02 | 1.0E-02 | 18 | |
rs4717806 | 0.776 | 0.200 | 7 | 73702147 | intron variant | T/A;C | snv | 9 | |||
rs3764650 | 0.790 | 0.200 | 19 | 1046521 | intron variant | T/G | snv | 0.14 | 9 | ||
rs363050 | 0.790 | 0.240 | 20 | 10253609 | intron variant | G/A | snv | 0.57 | 8 | ||
rs2298813 | 0.790 | 0.120 | 11 | 121522975 | missense variant | G/A;T | snv | 7.2E-02; 4.0E-06 | 7 | ||
rs972936 | 0.807 | 0.200 | 12 | 102431143 | intron variant | T/C | snv | 0.70 | 12 | ||
rs104894103 | 0.807 | 0.280 | 9 | 32974495 | stop gained | C/G;T | snv | 4.0E-06; 1.6E-04 | 6 | ||
rs754203 | 0.807 | 0.200 | 14 | 99691630 | non coding transcript exon variant | A/G | snv | 0.27 | 6 | ||
rs7354779 | 0.827 | 0.200 | 21 | 44250887 | missense variant | T/C | snv | 0.21 | 6 | ||
rs9331888 | 0.827 | 0.200 | 8 | 27611345 | 5 prime UTR variant | C/G | snv | 0.35 | 0.28 | 5 | |
rs669 | 0.851 | 0.080 | 12 | 9079672 | missense variant | T/C | snv | 0.31 | 0.33 | 7 | |
rs610932 | 0.851 | 0.080 | 11 | 60171834 | downstream gene variant | T/G | snv | 0.57 | 5 | ||
rs8702 | 0.851 | 0.160 | 14 | 103686015 | 3 prime UTR variant | C/G | snv | 0.61 | 5 | ||
rs11637611 | 0.851 | 0.160 | 15 | 72259371 | intron variant | C/T | snv | 0.63 | 4 | ||
rs12344615 | 0.851 | 0.080 | 9 | 83666280 | intron variant | A/C;G | snv | 4 | |||
rs12752888 | 0.851 | 0.160 | 1 | 54527266 | downstream gene variant | T/C | snv | 0.26 | 4 | ||
rs2070045 | 0.851 | 0.080 | 11 | 121577381 | synonymous variant | T/G | snv | 0.32 | 0.23 | 4 | |
rs541458 | 0.851 | 0.080 | 11 | 86077309 | regulatory region variant | C/T | snv | 0.71 | 4 | ||
rs59007384 | 0.851 | 0.080 | 19 | 44893408 | intron variant | G/A;T | snv | 4 | |||
rs7840202 | 0.851 | 0.160 | 8 | 102296172 | intron variant | A/C | snv | 0.21 | 4 | ||
rs9357347 | 0.851 | 0.080 | 6 | 41182853 | intergenic variant | A/C;T | snv | 4 | |||
rs11767557 | 0.882 | 0.080 | 7 | 143412046 | intron variant | T/C | snv | 0.18 | 4 | ||
rs11887120 | 0.882 | 0.080 | 2 | 25262866 | intron variant | C/T | snv | 0.45 | 4 |