Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4676410 0.716 0.240 2 240624322 intron variant G/A snv 0.26 17
rs3749171 0.807 0.120 2 240630275 missense variant C/T snv 0.16; 9.4E-06 0.19 6
rs34236350 2 240628909 5 prime UTR variant C/T snv 0.25 2
rs3749172 1.000 0.040 2 240630832 missense variant A/C;T snv 0.56; 2.0E-05 1