Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs3765524 0.724 0.320 10 94298541 missense variant C/T snv 0.27 0.31 17
rs1800875 0.742 0.360 14 24510132 upstream gene variant C/T snv 0.41 12
rs3740360 0.827 0.240 10 94265734 intron variant A/C snv 9.7E-02 8.4E-02 7
rs3132468 0.827 0.240 6 31507709 intron variant C/T snv 0.77 5