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
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66