Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1635 1.000 0.040 6 28259826 missense variant C/A;T snv 0.12 1
rs17720293 1.000 0.040 6 28246920 intron variant C/T snv 6.4E-02 7.2E-02 1