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
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs375752214 0.708 0.400 7 150998541 missense variant C/T snv 4.1E-06 4.2E-05 22
rs9349379 0.732 0.200 6 12903725 intron variant A/G snv 0.32 19