Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12646351 | 0.790 | 0.080 | 4 | 145819473 | intron variant | G/A | snv | 0.19 | 10 | ||
rs17806780 | 0.790 | 0.080 | 4 | 145811502 | intron variant | T/C | snv | 0.18 | 10 | ||
rs4835265 | 4 | 145900258 | intron variant | C/A | snv | 0.15 | 6 | ||||
rs11930385 | 4 | 145924600 | intron variant | C/T | snv | 0.51 | 1 | ||||
rs12331851 | 1.000 | 0.040 | 4 | 145928143 | intron variant | G/A | snv | 7.1E-02 | 1 | ||
rs2048161 | 4 | 145932013 | intron variant | A/C;G | snv | 1 | |||||
rs35146602 | 4 | 145866089 | intron variant | A/G | snv | 0.15 | 1 | ||||
rs35879803 | 1.000 | 0.040 | 4 | 145861685 | non coding transcript exon variant | C/A;T | snv | 1 | |||
rs4345206 | 1.000 | 0.040 | 4 | 145845384 | intron variant | T/C | snv | 0.59 | 1 | ||
rs4547811 | 4 | 145873469 | intron variant | T/C | snv | 0.20 | 1 | ||||
rs4835266 | 4 | 145900573 | intron variant | T/A;C | snv | 1 | |||||
rs7666150 | 4 | 145893488 | intron variant | T/C | snv | 0.54 | 1 |