Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7330914 13 110274714 intron variant C/A snv 3.0E-02 3
rs7998875 13 110289053 intron variant G/A;T snv 3
rs4773144 0.827 0.080 13 110308365 intron variant A/G snv 0.42 3
rs3809346 1.000 0.080 13 110308596 intron variant G/A;C snv 2
rs494558 13 110276815 intron variant C/T snv 0.90 1
rs3742207 0.925 0.120 13 110166251 missense variant T/A;G snv 2.8E-05; 0.30 1
rs11617955 1.000 0.040 13 110165755 intron variant T/A snv 9.3E-02 1
rs12873154 1.000 0.040 13 110268505 intron variant A/G snv 8.7E-02 1