Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1799971 | 0.559 | 0.600 | 6 | 154039662 | missense variant | A/G | snv | 0.19 | 0.12 | 95 | |
rs6313 | 0.562 | 0.640 | 13 | 46895805 | synonymous variant | G/A | snv | 0.41 | 0.40 | 82 | |
rs1800497 | 0.620 | 0.400 | 11 | 113400106 | missense variant | G/A | snv | 0.26 | 0.26 | 56 | |
rs1611115 | 0.732 | 0.280 | 9 | 133635393 | upstream gene variant | T/C | snv | 0.80 | 16 | ||
rs6065904 | 1.000 | 0.080 | 20 | 45906012 | intron variant | G/A | snv | 0.23 | 7 | ||
rs1106076 | 1.000 | 0.080 | 7 | 5581212 | regulatory region variant | C/A;G | snv | 2 | |||
rs12305135 | 1.000 | 0.080 | 12 | 130150660 | non coding transcript exon variant | T/C | snv | 6.8E-02 | 2 | ||
rs10812227 | 1.000 | 0.080 | 9 | 2548556 | intron variant | C/G;T | snv | 2 | |||
rs201815520 | 1.000 | 0.080 | 6 | 77463302 | synonymous variant | G/A | snv | 1.4E-05 | 1 |