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
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 169
rs9651118 0.683 0.480 1 11802157 intron variant T/C snv 0.18 20
rs1537514 0.882 0.120 1 11788011 missense variant G/C snv 0.10 0.10 4