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
rs10994359 0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 3
rs4624519 0.925 0.040 3 36821489 intron variant C/A;G;T snv 0.37 2
rs6550435 0.925 0.040 3 36822998 upstream gene variant T/G snv 0.38 2