Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4765127 12 123975620 intron variant G/T snv 0.33 2
rs7307277 12 123990609 intron variant A/G snv 0.32 2
rs11057408 12 123980289 intron variant G/T snv 0.33 1
rs12310367 12 124002131 intron variant A/G snv 0.33 1