Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs531184891 11 67129907 intron variant AA/-;A;AAA delins 5.0E-02 3
rs7952436 11 67257063 3 prime UTR variant C/T snv 4.7E-02 3
rs12785905 1.000 0.080 11 67184494 intron variant G/C snv 3.4E-02 1
rs552846225 11 67145999 intron variant T/-;TT;TTT delins 1
rs56088284 11 67132148 intron variant A/G snv 4.8E-02 1