Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11734460 4 711285 intron variant C/A;T snv 4
rs79839061 4 712095 intron variant G/A snv 9.6E-02 1
rs56011263 4 709183 intron variant T/C snv 0.35 1
rs75751670 4 707252 intron variant G/A snv 0.10 1
rs79713586 4 735866 intron variant A/T snv 6.4E-02 1
rs142708984 4 707538 intron variant C/A;T snv 1