Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11055980 1.000 0.040 12 14458588 intron variant C/T snv 0.40 2
rs10845988 12 14368248 intron variant T/C snv 0.40 1
rs4764094 12 14490783 intron variant T/G snv 0.57 1
rs7313259 12 14475839 intron variant C/T snv 0.47 0.42 1