Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28934575 0.641 0.400 17 7674230 missense variant C/A;G;T snv 25
rs121912660 0.683 0.240 17 7673781 missense variant C/A;G;T snv 18
rs78378222 0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 17
rs35850753 0.807 0.080 17 7675353 5 prime UTR variant C/T snv 1.3E-02 6
rs1625895 0.752 0.200 17 7674797 non coding transcript exon variant T/A;C;G snv 9.1E-06; 0.86; 4.5E-06 3
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 1
rs55819519 0.627 0.400 17 7673751 missense variant C/A;G;T snv 1.6E-04 1.3E-04 1