Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121913287 | 0.752 | 0.400 | 3 | 179199088 | missense variant | G/A | snv | 12 | |||
rs1057519933 | 0.790 | 0.240 | 3 | 179199156 | missense variant | A/G | snv | 11 | |||
rs1057519934 | 0.790 | 0.240 | 3 | 179199158 | missense variant | G/C | snv | 11 | |||
rs1057519935 | 0.790 | 0.240 | 3 | 179199157 | missense variant | A/G | snv | 11 | |||
rs1057519936 | 0.776 | 0.200 | 3 | 179234284 | missense variant | A/G;T | snv | 11 | |||
rs1057519937 | 0.776 | 0.200 | 3 | 179234285 | missense variant | T/C | snv | 11 | |||
rs121913284 | 0.776 | 0.160 | 3 | 179203765 | missense variant | T/A;G | snv | 11 | |||
rs2699887 | 0.763 | 0.280 | 3 | 179148620 | intron variant | C/T | snv | 0.18 | 11 | ||
rs1057519926 | 0.776 | 0.200 | 3 | 179210293 | missense variant | A/T | snv | 10 | |||
rs1057519929 | 0.776 | 0.320 | 3 | 179199066 | missense variant | G/A | snv | 10 | |||
rs1057519938 | 0.776 | 0.160 | 3 | 179203764 | missense variant | A/C;T | snv | 10 | |||
rs1057519939 | 0.776 | 0.160 | 3 | 179203763 | missense variant | A/C | snv | 10 | |||
rs1057519941 | 0.776 | 0.240 | 3 | 179203761 | missense variant | T/C;G | snv | 10 | |||
rs867262025 | 0.790 | 0.360 | 3 | 179221146 | missense variant | G/A | snv | 10 | |||
rs1057519928 | 0.807 | 0.200 | 3 | 179221147 | missense variant | A/C | snv | 8 | |||
rs17849071 | 0.776 | 0.160 | 3 | 179218439 | intron variant | T/G | snv | 7.9E-02 | 8 | ||
rs6443624 | 0.776 | 0.200 | 3 | 179179886 | intron variant | C/A | snv | 0.30 | 8 | ||
rs749415085 | 0.807 | 0.160 | 3 | 179198937 | missense variant | C/A;G;T | snv | 7 | |||
rs1057519931 | 0.827 | 0.160 | 3 | 179199141 | missense variant | G/C | snv | 6 | |||
rs863225460 | 0.882 | 0.200 | 3 | 179199160 | missense variant | T/A | snv | 5 | |||
rs121913277 | 0.925 | 0.280 | 3 | 179234302 | missense variant | G/A;C | snv | 4 | |||
rs121913282 | 0.882 | 0.040 | 3 | 179221072 | missense variant | A/C | snv | 4 | |||
rs397517202 | 0.851 | 0.320 | 3 | 179234230 | missense variant | A/G | snv | 4 | |||
rs6443626 | 0.851 | 0.200 | 3 | 179237995 | 3 prime UTR variant | T/C | snv | 0.24 | 4 | ||
rs7646409 | 0.882 | 0.040 | 3 | 179182405 | intron variant | T/C | snv | 0.26 | 4 |