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
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs3743930 0.611 0.720 16 3254626 missense variant C/G;T snv 7.1E-02 43
rs3819025 0.752 0.480 6 52186476 intron variant G/A snv 0.13 8.5E-02 11
rs1800897 0.925 0.240 10 100809115 synonymous variant C/T snv 7.4E-02 0.13 2