Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11860650 0.882 0.120 16 31315385 intron variant C/T snv 0.14 2
rs1143679 0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 1
rs12928725 1.000 0.080 16 31272675 intron variant G/A;T snv 1
rs34572943 1.000 0.080 16 31261032 intron variant G/A snv 0.11 1
rs35472514 1.000 0.080 16 31272002 intron variant C/G;T snv 0.12 0.12 1
rs9888739 0.882 0.120 16 31301932 intron variant C/T snv 0.26 1