Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10744826 | 12 | 109527707 | intron variant | C/G | snv | 0.57 | 3 | ||||
rs4841465 | 8 | 10962344 | intron variant | C/G;T | snv | 3 | |||||
rs11102001 | 0.925 | 0.080 | 1 | 109757069 | missense variant | G/A | snv | 9.4E-02 | 0.16 | 2 | |
rs4260308 | 20 | 10981537 | intron variant | G/A | snv | 0.41 | 2 | ||||
rs6108787 | 20 | 10986566 | intron variant | T/G | snv | 0.46 | 5 | ||||
rs143020224 | 19 | 11076648 | intron variant | C/G;T | snv | 2 | |||||
rs10849915 | 0.925 | 0.080 | 12 | 110895818 | intron variant | T/C | snv | 0.39 | 2 | ||
rs12229654 | 0.763 | 0.320 | 12 | 110976657 | intergenic variant | T/G | snv | 4.8E-03 | 7 | ||
rs1265564 | 1.000 | 0.120 | 12 | 111270654 | non coding transcript exon variant | A/C | snv | 0.30 | 4 | ||
rs7310615 | 0.882 | 12 | 111427245 | intron variant | C/G | snv | 0.67 | 12 | |||
rs7137828 | 0.763 | 0.200 | 12 | 111494996 | intron variant | C/A;T | snv | 14 | |||
rs597808 | 0.742 | 0.200 | 12 | 111535554 | intron variant | A/G | snv | 0.67 | 19 | ||
rs11065979 | 0.851 | 0.200 | 12 | 111621753 | intergenic variant | C/T | snv | 0.30 | 12 | ||
rs3782886 | 0.724 | 0.480 | 12 | 111672685 | synonymous variant | T/C | snv | 1.9E-02 | 5.9E-03 | 5 | |
rs11066015 | 0.925 | 0.120 | 12 | 111730205 | intron variant | G/A | snv | 5.9E-03 | 3 | ||
rs2013002 | 12 | 111762346 | intron variant | T/A;C | snv | 5 | |||||
rs671 | 0.529 | 0.840 | 12 | 111803962 | missense variant | G/A | snv | 1.9E-02 | 5.8E-03 | 21 | |
rs11513729 | 1.000 | 0.080 | 12 | 111835695 | downstream gene variant | C/T | snv | 0.29 | 5 | ||
rs4767293 | 12 | 112025492 | downstream gene variant | A/G | snv | 0.53 | 2 | ||||
rs17696736 | 0.827 | 0.240 | 12 | 112049014 | intron variant | A/G | snv | 0.30 | 12 | ||
rs7096937 | 10 | 112190660 | intron variant | T/C | snv | 0.72 | 5 | ||||
rs2074356 | 0.763 | 0.280 | 12 | 112207597 | intron variant | G/A | snv | 3.8E-03 | 9 | ||
rs7953257 | 12 | 112246417 | intron variant | A/G;T | snv | 0.71 | 5 | ||||
rs10741534 | 11 | 11233360 | intergenic variant | T/A;C | snv | 2 | |||||
rs11066280 | 0.742 | 0.280 | 12 | 112379979 | intron variant | T/A | snv | 7.0E-03 | 13 |