Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2076295
DSP
0.882 0.080 6 7562999 intron variant T/G snv 0.46 3
rs2744371
DSP
0.925 0.080 6 7553941 intron variant A/C;G snv 2