Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs62621409 11 36437447 missense variant A/G snv 3.9E-02 3.5E-02 3
rs11603150 11 36352319 intron variant T/C snv 0.25 1
rs67184556 11 36306244 intron variant C/T snv 0.30 1
rs7114403 11 36340057 intron variant T/A;G snv 1