Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs13107325 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 20
rs4841132 8 9326086 non coding transcript exon variant A/G snv 0.89 14