Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1047891 0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 25
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 25
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 21
rs597808 0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 18
rs198851 6 26104404 downstream gene variant T/A;C;G snv 11