Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2069825 | 1.000 | 0.040 | 7 | 22725718 | non coding transcript exon variant | -/CC | delins | 6.7E-05 | 2 | ||
rs2069837 | 0.724 | 0.520 | 7 | 22728408 | intron variant | A/C;G | snv | 18 | |||
rs1800797 | 0.605 | 0.800 | 7 | 22726602 | non coding transcript exon variant | A/G | snv | 0.72 | 43 | ||
rs747126003 | 0.689 | 0.400 | 7 | 22728790 | missense variant | A/G;T | snv | 4.0E-06 | 18 | ||
rs2069832 | 0.851 | 0.200 | 7 | 22727814 | intron variant | A/G;T | snv | 4 | |||
rs777906302 | 0.925 | 0.160 | 7 | 22728782 | synonymous variant | A/G;T | snv | 4.0E-06 | 3 | ||
rs1474347 | 1.000 | 0.120 | 7 | 22728505 | non coding transcript exon variant | C/A | snv | 0.69 | 1 | ||
rs2069861 | 0.925 | 0.080 | 7 | 22732035 | upstream gene variant | C/A;T | snv | 2 | |||
rs1800795 | 0.494 | 0.840 | 7 | 22727026 | intron variant | C/G | snv | 0.71 | 140 | ||
rs2069840 | 0.742 | 0.360 | 7 | 22728953 | intron variant | C/G | snv | 0.27 | 13 | ||
rs1474348 | 0.882 | 0.080 | 7 | 22728289 | intron variant | C/G | snv | 0.71 | 4 | ||
rs2069849 | 0.882 | 0.120 | 7 | 22731537 | missense variant | C/G;T | snv | 4.4E-02 | 3 | ||
rs1524107 | 0.827 | 0.320 | 7 | 22728600 | non coding transcript exon variant | C/T | snv | 9.4E-02 | 6 | ||
rs2069845 | 0.807 | 0.120 | 7 | 22730530 | intron variant | G/A | snv | 0.61 | 8 | ||
rs13306436 | 7 | 22731677 | 3 prime UTR variant | G/A | snv | 7.2E-04 | 3 | ||||
rs2069843 | 1.000 | 0.040 | 7 | 22730375 | intron variant | G/A | snv | 5.6E-02 | 1 | ||
rs1800796 | 0.555 | 0.760 | 7 | 22726627 | non coding transcript exon variant | G/C | snv | 9.9E-02 | 74 | ||
rs2069827 | 1.000 | 0.040 | 7 | 22725837 | non coding transcript exon variant | G/C;T | snv | 1 | |||
rs2066992 | 0.807 | 0.200 | 7 | 22728630 | non coding transcript exon variant | G/T | snv | 9.4E-02 | 6 | ||
rs13306435 | 1.000 | 0.080 | 7 | 22731420 | missense variant | T/A;C | snv | 2.9E-02; 4.2E-06 | 1 | ||
rs1554606 | 0.925 | 0.120 | 7 | 22729088 | intron variant | T/A;G | snv | 2 | |||
rs369953112 | 1.000 | 0.040 | 7 | 22731416 | missense variant | T/C | snv | 1 |