Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs79105258 | 12 | 111280427 | intron variant | C/A;T | snv | 23 | |||||
rs4841132 | 8 | 9326086 | non coding transcript exon variant | A/G | snv | 0.89 | 14 | ||||
rs7776054 | 6 | 135097778 | intron variant | A/G | snv | 0.24 | 13 | ||||
rs7310615 | 0.882 | 12 | 111427245 | intron variant | C/G | snv | 0.67 | 12 | |||
rs2954031 | 8 | 125479491 | intron variant | G/T | snv | 0.42 | 8 | ||||
rs4418728 | 10 | 93079967 | downstream gene variant | G/T | snv | 0.42 | 8 | ||||
rs4665972 | 2 | 27375230 | intron variant | T/C | snv | 0.69 | 8 | ||||
rs740746 | 10 | 114033028 | intergenic variant | G/A | snv | 0.70 | 8 | ||||
rs112875651 | 8 | 125494452 | intron variant | G/A | snv | 0.31 | 7 | ||||
rs13108218 | 4 | 3442204 | intron variant | A/G;T | snv | 7 | |||||
rs2001945 | 8 | 125465736 | upstream gene variant | G/A;C;T | snv | 7 | |||||
rs9376090 | 6 | 135090090 | intron variant | T/C | snv | 0.19 | 7 | ||||
rs10408163 | 19 | 47093845 | non coding transcript exon variant | T/C | snv | 0.52 | 6 | ||||
rs10808546 | 8 | 125483576 | intron variant | C/T | snv | 0.39 | 6 | ||||
rs112259268 | 17 | 43797377 | downstream gene variant | C/A | snv | 1.9E-02 | 6 | ||||
rs174529 | 11 | 61776489 | intron variant | T/C | snv | 0.34 | 6 | ||||
rs174551 | 11 | 61806212 | 5 prime UTR variant | T/C | snv | 0.28 | 6 | ||||
rs2169387 | 8 | 9323885 | intron variant | A/G | snv | 0.87 | 6 | ||||
rs2575876 | 9 | 104903458 | intron variant | G/A | snv | 0.24 | 6 | ||||
rs2642438 | 1 | 220796686 | missense variant | A/G | snv | 0.75 | 0.78 | 6 | |||
rs77303550 | 16 | 72045758 | intron variant | C/T | snv | 0.19 | 6 | ||||
rs10832027 | 11 | 13335636 | intron variant | G/A | snv | 0.67 | 5 | ||||
rs1129555 | 10 | 112150963 | 3 prime UTR variant | A/G | snv | 0.71 | 5 | ||||
rs114165349 | 1 | 26695422 | intron variant | G/C | snv | 1.7E-02 | 5 | ||||
rs127430 | 20 | 58589799 | intron variant | A/G;T | snv | 5 |