Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1131691014 | 0.439 | 0.800 | 17 | 7676154 | frameshift variant | -/C | ins | 214 | |||
rs878854066 | 0.439 | 0.800 | 17 | 7676153 | missense variant | GG/AC | mnv | 213 | |||
rs10069690 | 0.595 | 0.560 | 5 | 1279675 | intron variant | C/T | snv | 0.36 | 53 | ||
rs2981582 | 0.695 | 0.360 | 10 | 121592803 | intron variant | A/G | snv | 0.58 | 21 | ||
rs13387042 | 0.732 | 0.280 | 2 | 217041109 | intergenic variant | A/G | snv | 0.44 | 16 | ||
rs10941679 | 0.763 | 0.120 | 5 | 44706396 | intergenic variant | A/G | snv | 0.25 | 11 | ||
rs2016347 | 0.790 | 0.160 | 15 | 98960571 | 3 prime UTR variant | G/A;T | snv | 9 | |||
rs2981579 | 0.776 | 0.280 | 10 | 121577821 | intron variant | A/G | snv | 0.53 | 8 | ||
rs4442975 | 0.827 | 0.120 | 2 | 217056046 | intergenic variant | G/T | snv | 0.47 | 7 | ||
rs4849887 | 0.807 | 0.080 | 2 | 120487546 | intergenic variant | T/A;C | snv | 7 | |||
rs4973768 | 0.807 | 0.120 | 3 | 27374522 | 3 prime UTR variant | C/T | snv | 0.44 | 7 | ||
rs12443621 | 0.807 | 0.120 | 16 | 52514125 | intron variant | A/G | snv | 0.48 | 6 | ||
rs10771399 | 0.827 | 0.080 | 12 | 28002147 | intergenic variant | A/G | snv | 8.9E-02 | 5 | ||
rs16917302 | 0.851 | 0.080 | 10 | 62501439 | intron variant | A/C | snv | 0.18 | 5 | ||
rs10822013 | 0.851 | 0.080 | 10 | 62492218 | intron variant | C/T | snv | 0.42 | 4 | ||
rs1292011 | 0.851 | 0.080 | 12 | 115398717 | regulatory region variant | A/G | snv | 0.43 | 4 | ||
rs13689 | 0.851 | 0.120 | 16 | 68834619 | 3 prime UTR variant | T/A;C;G | snv | 4 | |||
rs1432679 | 0.851 | 0.080 | 5 | 158817075 | intron variant | C/T | snv | 0.44 | 4 | ||
rs192876988 | 0.851 | 0.120 | 4 | 79376097 | intergenic variant | T/C | snv | 1.6E-02 | 4 | ||
rs6828523 | 0.851 | 0.080 | 4 | 174925275 | intron variant | C/A | snv | 0.20 | 4 | ||
rs704010 | 0.851 | 0.080 | 10 | 79081391 | intron variant | T/C | snv | 0.71 | 4 | ||
rs865686 | 0.851 | 0.080 | 9 | 108126198 | regulatory region variant | G/A;T | snv | 4 | |||
rs981782 | 0.851 | 0.080 | 5 | 45285616 | intron variant | A/C | snv | 0.34 | 4 | ||
rs13267382 | 0.882 | 0.080 | 8 | 116197325 | intron variant | A/G | snv | 0.45 | 3 | ||
rs2268578 | 0.882 | 0.080 | 12 | 91107421 | intron variant | A/G | snv | 0.71 | 3 |