Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3774427 3 53531601 intron variant C/G snv 0.11 4
rs9814480 3 53556438 intron variant C/T snv 0.14 4
rs3821843 3 53523985 intron variant G/A snv 0.72 3
rs9810888 3 53601568 intron variant T/G snv 0.51 3
rs3774447 3 53561685 intron variant T/C snv 2.9E-02 2
rs9821489 3 53541701 intron variant G/A snv 0.16 1