Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4135385 0.742 0.320 3 41237949 non coding transcript exon variant A/G snv 0.19 14
rs2293303 0.827 0.200 3 41239336 synonymous variant C/T snv 3.2E-02 1.2E-02 7
rs11564475 0.882 0.080 3 41238542 intron variant A/G snv 3.7E-02 3
rs1880481 0.925 0.080 3 41230590 intron variant C/A snv 0.40 2