Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6993770 | 0.925 | 0.080 | 8 | 105569300 | intron variant | A/T | snv | 0.31 | 9 | ||
rs10761731 | 10 | 63267850 | intron variant | A/T | snv | 0.38 | 6 | ||||
rs2375980 | 9 | 2692622 | intergenic variant | C/G | snv | 0.51 | 3 | ||||
rs113600793 | 17 | 47384095 | intron variant | C/A;T | snv | 3 | |||||
rs2393967 | 10 | 63373396 | intron variant | A/C | snv | 0.23 | 3 | ||||
rs4349809 | 6 | 43957093 | intergenic variant | T/A;G | snv | 2 | |||||
rs145593549 | 6 | 44160144 | intron variant | A/T | snv | 6.8E-03 | 2 | ||||
rs2893923 | 10 | 63501424 | intron variant | C/T | snv | 0.27 | 2 | ||||
rs12199215 | 6 | 44059177 | non coding transcript exon variant | C/T | snv | 0.25 | 2 | ||||
rs72831623 | 17 | 47644927 | intron variant | G/A;C | snv | 4.0E-02 | 2 | ||||
rs192137842 | 9 | 107505575 | regulatory region variant | G/A | snv | 1.3E-03 | 1 |