Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10038113 | 1.000 | 0.040 | 5 | 25902233 | intergenic variant | T/C | snv | 0.45 | 1 | ||
rs10058083 | 1.000 | 0.040 | 5 | 25894289 | intergenic variant | G/A | snv | 0.38 | 1 | ||
rs1006737 | 0.695 | 0.120 | 12 | 2236129 | intron variant | G/A | snv | 0.36 | 27 | ||
rs10185592 | 1.000 | 0.040 | 2 | 205829457 | intergenic variant | A/C | snv | 0.11 | 1 | ||
rs10205350 | 1.000 | 0.040 | 2 | 30923631 | intron variant | G/T | snv | 0.24 | 1 | ||
rs10239799 | 1.000 | 0.040 | 7 | 120765281 | intergenic variant | C/T | snv | 0.37 | 1 | ||
rs10489525 | 1.000 | 0.040 | 1 | 114721064 | intron variant | G/A | snv | 0.32 | 1 | ||
rs10498676 | 0.925 | 0.040 | 6 | 11026766 | intron variant | G/A | snv | 0.18 | 3 | ||
rs10500171 | 1.000 | 0.040 | 7 | 147183313 | intron variant | A/G | snv | 0.52 | 1 | ||
rs10513025 | 1.000 | 0.040 | 5 | 9623510 | non coding transcript exon variant | T/C | snv | 5.4E-02 | 1 | ||
rs1051312 | 0.827 | 0.120 | 20 | 10306440 | 3 prime UTR variant | T/C | snv | 0.20 | 5 | ||
rs1053972 | 1.000 | 0.040 | 19 | 50855373 | 3 prime UTR variant | C/T | snv | 0.24 | 1 | ||
rs1057518345 | 0.742 | 0.400 | 20 | 50894172 | frameshift variant | ACTA/- | delins | 25 | |||
rs1057518658 | 1.000 | 0.040 | 2 | 165331409 | frameshift variant | AC/- | del | 1 | |||
rs1057518993 | 1.000 | 0.040 | X | 53243367 | stop gained | G/A | snv | 1 | |||
rs1057518999 | 1.000 | 0.040 | 3 | 70977826 | splice donor variant | A/G | snv | 1 | |||
rs1057519440 | 1.000 | 0.040 | X | 51744647 | missense variant | G/A | snv | 3 | |||
rs1057521223 | 1.000 | 0.040 | 2 | 165373339 | stop gained | G/A;T | snv | 5 | |||
rs1060499733 | 0.851 | 0.120 | 3 | 47846757 | missense variant | A/G | snv | 11 | |||
rs1060826 | 0.851 | 0.160 | 17 | 27762841 | synonymous variant | T/C | snv | 0.66 | 0.67 | 4 | |
rs1064793345 | 0.752 | 0.240 | 10 | 87961039 | missense variant | T/C | snv | 11 | |||
rs1064794245 | 1.000 | 0.040 | 22 | 40349918 | missense variant | A/C | snv | 1 | |||
rs1064794254 | 0.851 | 0.120 | X | 119841185 | frameshift variant | CT/- | delins | 6 | |||
rs10732392 | 1.000 | 0.040 | 9 | 126633758 | intron variant | A/G | snv | 0.84 | 1 | ||
rs10749886 | 1.000 | 0.040 | 11 | 107129809 | intergenic variant | G/A | snv | 0.35 | 1 |