Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 262 | |
rs1799945 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 226 | |
rs855791 | 0.701 | 0.400 | 22 | 37066896 | missense variant | A/G;T | snv | 0.57; 4.0E-06 | 38 | ||
rs11065987 | 0.807 | 0.280 | 12 | 111634620 | intergenic variant | A/G | snv | 0.29 | 17 | ||
rs198851 | 6 | 26104404 | downstream gene variant | T/A;C;G | snv | 15 | |||||
rs4820268 | 0.851 | 0.160 | 22 | 37073551 | missense variant | G/A;C | snv | 0.53; 4.0E-06 | 14 | ||
rs10224002 | 0.925 | 0.080 | 7 | 151717955 | intron variant | A/G | snv | 0.31 | 12 | ||
rs198846 | 6 | 26107235 | downstream gene variant | A/G;T | snv | 7 | |||||
rs129128 | 6 | 26125114 | intron variant | C/T | snv | 0.91 | 7 | ||||
rs130624 | 22 | 37042611 | regulatory region variant | G/T | snv | 0.47 | 6 | ||||
rs228129 | 22 | 37032558 | upstream gene variant | A/G | snv | 0.48 | 6 | ||||
rs2413450 | 22 | 37074184 | intron variant | T/C | snv | 0.61 | 6 | ||||
rs198833 | 6 | 26114280 | downstream gene variant | G/A | snv | 0.87 | 5 | ||||
rs10495928 | 2 | 46126027 | intron variant | A/G | snv | 0.36 | 5 | ||||
rs11089823 | 22 | 37113139 | upstream gene variant | T/C | snv | 0.28 | 4 | ||||
rs11089824 | 22 | 37113146 | upstream gene variant | A/C;T | snv | 4 | |||||
rs763668 | 22 | 37115036 | intergenic variant | C/G;T | snv | 4 | |||||
rs16926246 | 10 | 69333636 | intron variant | C/T | snv | 0.12 | 4 | ||||
rs5750373 | 22 | 37028990 | non coding transcript exon variant | G/A | snv | 0.49 | 4 | ||||
rs5756520 | 22 | 37112467 | upstream gene variant | G/A | snv | 0.41 | 4 | ||||
rs11914132 | 22 | 37113047 | upstream gene variant | C/T | snv | 0.27 | 3 | ||||
rs228918 | 22 | 37110640 | upstream gene variant | T/C | snv | 0.40 | 3 | ||||
rs228919 | 22 | 37110673 | upstream gene variant | G/T | snv | 0.40 | 3 | ||||
rs228921 | 22 | 37110836 | upstream gene variant | A/G | snv | 0.41 | 3 | ||||
rs6013509 | 20 | 52701812 | downstream gene variant | G/A;C | snv | 2 |