Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12272004 | 1.000 | 0.040 | 11 | 116733008 | TF binding site variant | C/A | snv | 9.8E-02 | 3 | ||
rs12670798 | 1.000 | 0.040 | 7 | 21567734 | intron variant | T/C | snv | 0.26 | 4 | ||
rs12740374 | 0.851 | 0.040 | 1 | 109274968 | 3 prime UTR variant | G/T | snv | 0.22 | 8 | ||
rs2156552 | 1.000 | 0.040 | 18 | 49655298 | downstream gene variant | A/G;T | snv | 4 | |||
rs4149268 | 1.000 | 0.040 | 9 | 104884939 | intron variant | C/T | snv | 0.46 | 4 | ||
rs4775041 | 1.000 | 0.040 | 15 | 58382496 | intron variant | G/C | snv | 0.24 | 7 | ||
rs6544713 | 0.925 | 0.040 | 2 | 43846742 | non coding transcript exon variant | T/C | snv | 0.75 | 5 | ||
rs10503669 | 0.925 | 0.080 | 8 | 19990179 | intergenic variant | C/A | snv | 8.4E-02 | 7 | ||
rs12678919 | 0.882 | 0.080 | 8 | 19986711 | intergenic variant | A/G | snv | 1.0E-01 | 7 | ||
rs1532085 | 0.882 | 0.080 | 15 | 58391167 | intron variant | A/G;T | snv | 9 | |||
rs6589566 | 0.882 | 0.080 | 11 | 116781707 | intron variant | G/A;C;T | snv | 7 | |||
rs6756629 | 0.925 | 0.080 | 2 | 43837951 | missense variant | G/A;T | snv | 6.7E-02 | 4 | ||
rs1122608 | 0.763 | 0.120 | 19 | 11052925 | intron variant | G/T | snv | 0.18 | 7 | ||
rs12654264 | 0.925 | 0.120 | 5 | 75352778 | intron variant | A/T | snv | 0.38 | 5 | ||
rs16996148 | 0.882 | 0.120 | 19 | 19547663 | downstream gene variant | G/T | snv | 0.10 | 5 | ||
rs1864163 | 0.882 | 0.120 | 16 | 56963321 | intron variant | G/A | snv | 0.26 | 8 | ||
rs1883025 | 0.807 | 0.120 | 9 | 104902020 | intron variant | C/T | snv | 0.28 | 7 | ||
rs3890182 | 0.925 | 0.120 | 9 | 104885374 | intron variant | G/A;T | snv | 4 | |||
rs629301 | 0.851 | 0.120 | 1 | 109275684 | 3 prime UTR variant | G/T | snv | 0.74 | 8 | ||
rs6511720 | 0.790 | 0.120 | 19 | 11091630 | intron variant | G/T | snv | 0.12 | 10 | ||
rs9989419 | 0.882 | 0.120 | 16 | 56951227 | regulatory region variant | A/G | snv | 0.55 | 8 | ||
rs1532624 | 0.851 | 0.160 | 16 | 56971567 | intron variant | C/A | snv | 0.34 | 7 | ||
rs157580 | 0.882 | 0.160 | 19 | 44892009 | intron variant | G/A | snv | 0.69 | 11 | ||
rs1800961 | 0.851 | 0.160 | 20 | 44413724 | missense variant | C/T | snv | 3.1E-02 | 2.5E-02 | 5 | |
rs2228671 | 0.790 | 0.160 | 19 | 11100236 | stop gained | C/A;G;T | snv | 1.6E-05; 8.9E-02 | 6 |