Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs1800797 0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs747126003 0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06 18
rs2069840 0.742 0.360 7 22728953 intron variant C/G snv 0.27 13