Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs4977574 0.695 0.520 9 22098575 intron variant A/G;T snv 26
rs1967309 0.925 0.080 16 4015582 non coding transcript exon variant A/G snv 0.51 3