Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2897075 | 1.000 | 0.040 | 7 | 100032719 | intron variant | C/T | snv | 0.31 | 1 | ||
rs7079679 | 1.000 | 0.040 | 10 | 100295789 | intron variant | C/A | snv | 0.57 | 1 | ||
rs2278843 | 1.000 | 0.040 | 10 | 100296751 | intron variant | A/G | snv | 0.58 | 1 | ||
rs12692398 | 0.925 | 0.080 | 2 | 10060189 | intron variant | G/A | snv | 0.17 | 2 | ||
rs633185 | 0.925 | 0.080 | 11 | 100722807 | intron variant | G/A;C | snv | 10 | |||
rs138886989 | 0.925 | 0.160 | X | 101401763 | missense variant | T/C | snv | 1.9E-04 | 2.8E-05 | 2 | |
rs56386186 | 1.000 | 0.040 | 14 | 102193651 | intron variant | T/C | snv | 9.7E-02 | 2 | ||
rs2071230 | 0.882 | 0.080 | 11 | 102790228 | 3 prime UTR variant | A/G | snv | 0.15 | 3 | ||
rs773474756 | 0.925 | 0.080 | 11 | 102790467 | missense variant | T/C | snv | 8.1E-06 | 2 | ||
rs1799750 | 0.592 | 0.760 | 11 | 102799765 | intron variant | C/- | delins | 0.50 | 48 | ||
rs470234 | 1.000 | 0.040 | 11 | 102811075 | intron variant | T/A;G | snv | 2 | |||
rs470928 | 1.000 | 0.040 | 11 | 102814649 | intron variant | G/A;T | snv | 2 | |||
rs470292 | 1.000 | 0.040 | 11 | 102814664 | intron variant | C/A | snv | 0.90 | 2 | ||
rs505987 | 1.000 | 0.040 | 11 | 102815179 | intron variant | A/G | snv | 0.89 | 2 | ||
rs475937 | 1.000 | 0.040 | 11 | 102816969 | intron variant | A/C;T | snv | 2 | |||
rs520146 | 1.000 | 0.040 | 11 | 102819400 | intron variant | T/C | snv | 0.90 | 2 | ||
rs564018 | 0.925 | 0.080 | 11 | 102820688 | intron variant | A/G;T | snv | 3 | |||
rs688258 | 1.000 | 0.040 | 11 | 102821364 | intron variant | A/C;T | snv | 2 | |||
rs595128 | 1.000 | 0.040 | 11 | 102822378 | intron variant | T/C | snv | 0.90 | 2 | ||
rs499459 | 0.925 | 0.080 | 11 | 102822455 | intron variant | A/G | snv | 0.90 | 3 | ||
rs611705 | 1.000 | 0.040 | 11 | 102823737 | intron variant | C/T | snv | 0.90 | 2 | ||
rs473238 | 1.000 | 0.040 | 11 | 102829629 | intron variant | T/C | snv | 0.90 | 2 | ||
rs553542 | 1.000 | 0.040 | 11 | 102830645 | intron variant | C/T | snv | 0.90 | 2 | ||
rs525119 | 1.000 | 0.040 | 11 | 102831415 | intron variant | G/T | snv | 0.90 | 2 | ||
rs646760 | 1.000 | 0.040 | 11 | 102832547 | non coding transcript exon variant | A/T | snv | 0.10 | 2 |