Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs16841143 | 2 | 208384849 | intron variant | G/A | snv | 0.13 | 2 | ||||
rs182087934 | 2 | 183742707 | intergenic variant | G/A | snv | 2 | |||||
rs384005 | 5 | 88709286 | intron variant | T/C | snv | 0.70 | 2 | ||||
rs4554696 | 1 | 65942328 | intron variant | C/T | snv | 0.33 | 2 | ||||
rs62199592 | 2 | 183858773 | intergenic variant | A/G | snv | 2.1E-02 | 2 | ||||
rs6475417 | 9 | 20212043 | intergenic variant | A/G;T | snv | 2 | |||||
rs6661750 | 1 | 66081201 | intron variant | A/G;T | snv | 2 | |||||
rs11123857 | 2 | 100987350 | non coding transcript exon variant | A/G | snv | 0.29 | 1 | ||||
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 5 | |
rs662 | 0.485 | 0.840 | 7 | 95308134 | missense variant | T/C | snv | 0.38 | 0.42 | 1 | |
rs1801253 | 0.683 | 0.440 | 10 | 114045297 | missense variant | G/C | snv | 0.74 | 0.69 | 6 | |
rs1006737 | 0.695 | 0.120 | 12 | 2236129 | intron variant | G/A | snv | 0.36 | 5 | ||
rs1344706 | 0.701 | 0.160 | 2 | 184913701 | intron variant | A/C;T | snv | 1 | |||
rs4625 | 0.716 | 0.280 | 3 | 49534707 | 3 prime UTR variant | A/G | snv | 0.30 | 17 | ||
rs2251219 | 0.732 | 0.120 | 3 | 52550771 | synonymous variant | T/C;G | snv | 0.39; 4.0E-06 | 0.34 | 1 | |
rs10994336 | 0.776 | 0.160 | 10 | 60420054 | intron variant | C/T | snv | 7.5E-02 | 1 | ||
rs11039149 | 0.827 | 0.280 | 11 | 47255124 | intron variant | A/G | snv | 0.19 | 2 | ||
rs7597593 | 0.827 | 0.160 | 2 | 184668853 | intron variant | T/C | snv | 0.53 | 2 | ||
rs12938031 | 0.851 | 0.160 | 17 | 45777136 | intron variant | A/G | snv | 0.26 | 4 | ||
rs7225002 | 0.925 | 0.080 | 17 | 46111701 | intron variant | A/G | snv | 0.39 | 5 | ||
rs9303521 | 0.925 | 0.120 | 17 | 45727828 | intron variant | T/C;G | snv | 0.60 | 5 | ||
rs62081501 | 0.925 | 0.080 | 18 | 37627749 | intron variant | G/A | snv | 6.2E-02 | 4 | ||
rs8067056 | 0.925 | 0.080 | 17 | 46006582 | intron variant | T/C;G | snv | 0.30 | 4 | ||
rs111365677 | 0.925 | 0.040 | 1 | 99463578 | upstream gene variant | T/C | snv | 2.3E-03 | 3 | ||
rs112106319 | 0.925 | 0.040 | 9 | 115094539 | intron variant | A/T | snv | 2.8E-03 | 3 |