Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs540635787 | 0.851 | 0.200 | 22 | 28694073 | missense variant | G/A;C;T | snv | 1.7E-05 | 4 | ||
rs212091 | 0.827 | 0.120 | 16 | 16142793 | 3 prime UTR variant | T/A;C | snv | 5 | |||
rs2239680 | 0.827 | 0.120 | 17 | 78223702 | 3 prime UTR variant | T/C | snv | 0.27 | 0.24 | 5 | |
rs3750861 | 0.827 | 0.120 | 10 | 3782241 | intron variant | C/T | snv | 8.2E-02 | 6.6E-02 | 5 | |
rs9915936 | 0.827 | 0.120 | 17 | 65537671 | synonymous variant | T/C | snv | 0.90 | 0.90 | 5 | |
rs1571801 | 0.827 | 0.120 | 9 | 121665094 | intron variant | G/T | snv | 0.21 | 6 | ||
rs2071203 | 0.827 | 0.120 | 3 | 50274469 | missense variant | C/T | snv | 0.12 | 9.9E-02 | 6 | |
rs2229388 | 0.807 | 0.120 | 8 | 16155139 | missense variant | G/A;C | snv | 4.0E-06; 0.11 | 7 | ||
rs2645429 | 0.790 | 0.120 | 8 | 11802542 | non coding transcript exon variant | A/G;T | snv | 7 | |||
rs17021918 | 0.776 | 0.240 | 4 | 94641726 | intron variant | C/T | snv | 0.30 | 8 | ||
rs8102476 | 0.776 | 0.240 | 19 | 38244973 | intron variant | C/T | snv | 0.40 | 8 | ||
rs1204382931 | 0.790 | 0.160 | 2 | 38075270 | missense variant | A/C | snv | 4.3E-06 | 10 | ||
rs760025060 | 0.776 | 0.200 | 2 | 38074936 | missense variant | C/T | snv | 10 | |||
rs7726159 | 0.790 | 0.160 | 5 | 1282204 | intron variant | C/A | snv | 0.29 | 10 | ||
rs7483 | 0.742 | 0.320 | 1 | 109737079 | missense variant | C/T | snv | 4.0E-06; 0.35 | 0.26 | 11 | |
rs2227284 | 0.732 | 0.480 | 5 | 132677033 | intron variant | T/C;G | snv | 12 | |||
rs2228526 | 0.752 | 0.200 | 10 | 49470671 | missense variant | T/C | snv | 0.22 | 0.19 | 13 | |
rs28360317 | 0.716 | 0.280 | 5 | 83323739 | intron variant | -/CCT | delins | 0.24 | 15 | ||
rs10012 | 0.716 | 0.280 | 2 | 38075247 | missense variant | G/C | snv | 0.31 | 0.36 | 16 | |
rs213950 | 0.716 | 0.320 | 7 | 117559479 | missense variant | G/A | snv | 0.47 | 0.57 | 16 | |
rs2242652 | 0.724 | 0.400 | 5 | 1279913 | intron variant | G/A | snv | 0.18 | 16 | ||
rs7003908 | 0.716 | 0.320 | 8 | 47858141 | intron variant | C/A | snv | 0.66 | 16 | ||
rs9350 | 0.742 | 0.240 | 1 | 241885372 | missense variant | C/T | snv | 0.21 | 0.19 | 16 | |
rs16901979 | 0.724 | 0.480 | 8 | 127112671 | intron variant | C/A | snv | 0.16 | 17 | ||
rs1202989817 | 0.716 | 0.360 | 21 | 31659813 | missense variant | T/C;G | snv | 8.0E-06 | 7.0E-06 | 18 |