Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs4073 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48