Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10408163 | 19 | 47093845 | non coding transcript exon variant | T/C | snv | 0.52 | 6 | ||||
rs1126930 | 12 | 49005349 | missense variant | G/C | snv | 2.1E-02 | 2.1E-02 | 5 | |||
rs12328675 | 2 | 164684290 | 3 prime UTR variant | T/C | snv | 0.13 | 4 | ||||
rs12967135 | 18 | 60181790 | intergenic variant | G/A | snv | 0.24 | 8 | ||||
rs2303108 | 19 | 47086638 | intron variant | T/C | snv | 0.63 | 3 | ||||
rs4691380 | 4 | 156798972 | intron variant | C/T | snv | 0.45 | 4 | ||||
rs4841132 | 8 | 9326086 | non coding transcript exon variant | A/G | snv | 0.89 | 14 | ||||
rs7621025 | 3 | 136553404 | intron variant | T/A;C | snv | 3 | |||||
rs7730898 | 5 | 171032671 | intron variant | G/A | snv | 0.75 | 2 | ||||
rs9942416 | 5 | 75741470 | intergenic variant | C/G | snv | 0.53 | 9 | ||||
rs998584 | 6 | 43790159 | downstream gene variant | C/A | snv | 0.41 | 11 | ||||
rs2257129 | 1.000 | 0.040 | 10 | 121139183 | regulatory region variant | T/C | snv | 0.82 | 3 | ||
rs2954021 | 1.000 | 0.040 | 8 | 125469835 | intron variant | A/G | snv | 0.54 | 15 | ||
rs823114 | 1.000 | 0.040 | 1 | 205750404 | upstream gene variant | G/A | snv | 0.45 | 3 | ||
rs11727676 | 0.776 | 0.080 | 4 | 144737912 | synonymous variant | T/C | snv | 6.6E-02 | 6.4E-02 | 14 | |
rs2296172 | 1.000 | 0.080 | 1 | 39370145 | missense variant | A/G;T | snv | 0.19; 8.0E-06 | 4 | ||
rs7607980 | 1.000 | 0.080 | 2 | 164694691 | missense variant | T/C | snv | 0.11 | 0.13 | 8 | |
rs9816226 | 1.000 | 0.080 | 3 | 186116710 | intron variant | A/T | snv | 0.82 | 5 | ||
rs10968576 | 0.882 | 0.120 | 9 | 28414341 | intron variant | A/G | snv | 0.26 | 10 | ||
rs12310617 | 0.851 | 0.120 | 12 | 3060327 | intergenic variant | C/T | snv | 0.11 | 16 | ||
rs12369179 | 0.851 | 0.120 | 12 | 122479003 | intron variant | C/T | snv | 5.9E-02 | 16 | ||
rs12420422 | 0.851 | 0.120 | 11 | 123009573 | intergenic variant | G/A | snv | 3.4E-02 | 16 | ||
rs12579302 | 0.851 | 0.120 | 12 | 89656726 | intron variant | A/G | snv | 0.15 | 19 | ||
rs13114738 | 0.851 | 0.120 | 4 | 102363708 | intron variant | C/A;T | snv | 16 | |||
rs1558902 | 0.827 | 0.120 | 16 | 53769662 | intron variant | T/A | snv | 0.31 | 21 |