Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 24 | ||
rs597808 | 0.742 | 0.200 | 12 | 111535554 | intron variant | A/G | snv | 0.67 | 19 | ||
rs28929474 | 0.708 | 0.320 | 14 | 94378610 | missense variant | C/G;T | snv | 2.8E-05; 1.1E-02 | 17 | ||
rs7903146 | 0.554 | 0.680 | 10 | 112998590 | intron variant | C/G;T | snv | 16 | |||
rs6567160 | 1.000 | 0.080 | 18 | 60161902 | upstream gene variant | T/C | snv | 0.21 | 8 | ||
rs7970350 | 12 | 65966384 | downstream gene variant | C/T | snv | 0.48 | 4 | ||||
rs8010717 | 14 | 79944098 | intron variant | T/C | snv | 0.29 | 4 | ||||
rs4947642 | 7 | 51797912 | intergenic variant | A/C;G | snv | 3 | |||||
rs7889 | 6 | 31637671 | 3 prime UTR variant | C/G | snv | 0.58 | 2 |