Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 6
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 5
rs10994359 0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 3
rs9371601 0.790 0.120 6 152469438 intron variant G/T snv 0.46 3
rs10994397 0.851 0.040 10 60519366 intron variant C/T snv 9.5E-02 2
rs12576775 0.827 0.080 11 79366149 intron variant A/G snv 0.15 2