Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1008723 | 0.925 | 0.160 | 17 | 39910014 | intron variant | G/C;T | snv | 3 | |||
rs10206753 | 1.000 | 0.080 | 2 | 102351902 | missense variant | T/C;G | snv | 0.34; 4.0E-06 | 2 | ||
rs1043828 | 1.000 | 0.080 | 5 | 111128310 | 3 prime UTR variant | T/C;G | snv | 2 | |||
rs12936231 | 0.925 | 0.160 | 17 | 39872867 | intron variant | C/G;T | snv | 3 | |||
rs1464510 | 0.807 | 0.280 | 3 | 188394766 | intron variant | C/A;T | snv | 7 | |||
rs17498196 | 1.000 | 0.080 | 9 | 6237547 | intron variant | A/C;G | snv | 2 | |||
rs1888909 | 0.882 | 0.200 | 9 | 6197392 | downstream gene variant | T/A;C | snv | 2 | |||
rs2066362 | 1.000 | 0.080 | 9 | 6219176 | intron variant | G/C;T | snv | 2 | |||
rs2872507 | 0.752 | 0.360 | 17 | 39884510 | intergenic variant | G/A;T | snv | 7 | |||
rs3771166 | 1.000 | 0.080 | 2 | 102369762 | intron variant | G/A;T | snv | 2 | |||
rs3771180 | 1.000 | 0.080 | 2 | 102337157 | 5 prime UTR variant | G/A;T | snv | 2 | |||
rs3939286 | 0.776 | 0.360 | 9 | 6210099 | regulatory region variant | T/A;C | snv | 2 | |||
rs4794820 | 0.790 | 0.160 | 17 | 39933091 | intron variant | A/G;T | snv | 3 | |||
rs4795405 | 0.851 | 0.160 | 17 | 39932164 | intron variant | T/A;C | snv | 3 | |||
rs8069176 | 0.882 | 0.080 | 17 | 39900944 | downstream gene variant | G/A;T | snv | 3 | |||
rs8076131 | 0.790 | 0.200 | 17 | 39924659 | intron variant | G/A;C | snv | 3 | |||
rs869402 | 0.925 | 0.160 | 17 | 39911790 | intron variant | T/A;C | snv | 3 | |||
rs928413 | 0.807 | 0.120 | 9 | 6213387 | upstream gene variant | G/A;C | snv | 2 | |||
rs9303280 | 1.000 | 0.080 | 17 | 39917778 | non coding transcript exon variant | T/A;C | snv | 2 | |||
rs992969 | 0.882 | 0.080 | 9 | 6209697 | intergenic variant | A/G;T | snv | 2 | |||
rs11692065 | 1.000 | 0.080 | 2 | 102267515 | intergenic variant | C/T | snv | 0.15 | 2 | ||
rs10189629 | 1.000 | 0.080 | 2 | 102263004 | regulatory region variant | C/A | snv | 0.15 | 2 | ||
rs11674302 | 1.000 | 0.080 | 2 | 102270668 | intergenic variant | T/C | snv | 0.16 | 2 | ||
rs10173081 | 1.000 | 0.080 | 2 | 102340888 | intron variant | C/T | snv | 0.18 | 2 | ||
rs13431828 | 0.925 | 0.160 | 2 | 102338193 | 5 prime UTR variant | C/T | snv | 0.18 | 2 |