Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4418728 | 10 | 93079967 | downstream gene variant | G/T | snv | 0.42 | 8 | ||||
rs1801689 | 17 | 66214462 | missense variant | A/C;G | snv | 4.0E-06; 2.4E-02; 4.8E-05 | 5 | ||||
rs7897379 | 10 | 63541965 | intron variant | T/C | snv | 0.43 | 3 | ||||
rs10508921 | 10 | 50250948 | intron variant | C/T | snv | 9.7E-02 | 2 | ||||
rs492602 | 0.925 | 0.120 | 19 | 48703160 | synonymous variant | A/G | snv | 0.38 | 0.45 | 6 | |
rs516246 | 0.925 | 0.160 | 19 | 48702915 | intron variant | C/T | snv | 0.38 | 0.45 | 10 | |
rs5167 | 1.000 | 0.040 | 19 | 44945208 | missense variant | T/A;G | snv | 3.6E-05; 0.39 | 4 | ||
rs5112 | 1.000 | 0.080 | 19 | 44927023 | non coding transcript exon variant | C/G | snv | 0.55 | 4 | ||
rs438811 | 19 | 44913484 | non coding transcript exon variant | C/T | snv | 0.29 | 5 | ||||
rs483082 | 1.000 | 0.080 | 19 | 44912921 | non coding transcript exon variant | G/T | snv | 0.28 | 3 | ||
rs75627662 | 1.000 | 0.080 | 19 | 44910319 | non coding transcript exon variant | C/T | snv | 0.17 | 3 | ||
rs7412 | 0.641 | 0.640 | 19 | 44908822 | missense variant | C/T | snv | 6.2E-02 | 7.9E-02 | 20 | |
rs429358 | 0.590 | 0.600 | 19 | 44908684 | missense variant | T/C | snv | 0.14 | 0.16 | 26 | |
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 55 | |
rs10864728 | 1 | 230169168 | intron variant | A/G | snv | 0.50 | 3 | ||||
rs4665710 | 2 | 20998163 | downstream gene variant | A/C | snv | 0.76 | 5 | ||||
rs495828 | 0.827 | 0.200 | 9 | 133279294 | upstream gene variant | T/G | snv | 0.81 | 11 | ||
rs964184 | 0.716 | 0.440 | 11 | 116778201 | 3 prime UTR variant | G/C | snv | 0.82 | 35 | ||
rs629301 | 0.851 | 0.120 | 1 | 109275684 | 3 prime UTR variant | G/T | snv | 0.74 | 19 |