Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2206593 | 0.925 | 0.080 | 1 | 186673297 | 3 prime UTR variant | A/G | snv | 0.95 | 3 | ||
rs6746030 | 0.763 | 0.320 | 2 | 166242648 | missense variant | A/G | snv | 0.88 | 0.88 | 16 | |
rs2070995 | 1.000 | 0.040 | 21 | 37714662 | synonymous variant | T/C | snv | 0.80 | 0.85 | 2 | |
rs2562456 | 1.000 | 0.040 | 19 | 21483408 | non coding transcript exon variant | C/T | snv | 0.77 | 2 | ||
rs887200 | 22 | 19976143 | intron variant | C/T | snv | 0.74 | 1 | ||||
rs1571138 | 1 | 46429969 | upstream gene variant | A/G | snv | 0.73 | 1 | ||||
rs1801253 | 0.683 | 0.440 | 10 | 114045297 | missense variant | G/C | snv | 0.74 | 0.69 | 34 | |
rs3800373 | 0.752 | 0.200 | 6 | 35574699 | 3 prime UTR variant | C/A | snv | 0.68 | 22 | ||
rs6801957 | 1.000 | 0.080 | 3 | 38725824 | intron variant | T/C | snv | 0.67 | 7 | ||
rs179971 | 6 | 16362511 | intron variant | C/T | snv | 0.66 | 1 | ||||
rs4660928 | 1 | 46420268 | TF binding site variant | A/C | snv | 0.63 | 1 | ||||
rs9524885 | 13 | 95283335 | intron variant | T/C | snv | 0.63 | 2 | ||||
rs4587017 | 4 | 69081680 | intron variant | T/G | snv | 0.63 | 1 | ||||
rs2073618 | 0.716 | 0.480 | 8 | 118951813 | missense variant | G/C | snv | 0.52 | 0.60 | 19 | |
rs2053044 | 1.000 | 0.040 | 5 | 148825809 | 5 prime UTR variant | A/G | snv | 0.59 | 5 | ||
rs6275 | 0.851 | 0.160 | 11 | 113412755 | synonymous variant | A/G | snv | 0.64 | 0.58 | 7 | |
rs7439366 | 0.752 | 0.320 | 4 | 69098620 | missense variant | T/C | snv | 0.56 | 0.57 | 16 | |
rs165599 | 0.677 | 0.280 | 22 | 19969258 | 3 prime UTR variant | G/A | snv | 0.56 | 27 | ||
rs8136867 | 0.882 | 0.080 | 22 | 21850504 | intron variant | G/A | snv | 0.55 | 4 | ||
rs6280 | 0.602 | 0.520 | 3 | 114171968 | missense variant | C/T | snv | 0.63 | 0.54 | 57 | |
rs6276 | 0.807 | 0.320 | 11 | 113410675 | 3 prime UTR variant | C/T | snv | 0.54 | 8 | ||
rs2756109 | 10 | 99798989 | intron variant | G/T | snv | 0.53 | 1 | ||||
rs398655 | 13 | 33013514 | upstream gene variant | A/C | snv | 0.51 | 1 | ||||
rs7718461 | 5 | 76962223 | intron variant | A/G | snv | 0.51 | 1 | ||||
rs2069718 | 0.742 | 0.320 | 12 | 68156382 | intron variant | A/G;T | snv | 0.50 | 14 |