Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12994997 1.000 0.040 2 233264857 intron variant G/A;C snv 0.45; 4.0E-06 2
rs6752107 1.000 0.040 2 233252802 intron variant G/A snv 0.44 2
rs2241880 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 1