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
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs352140 0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49 42
rs3748067 0.672 0.320 6 52190541 3 prime UTR variant C/T snv 6.2E-02 21