Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs55819519 0.627 0.400 17 7673751 missense variant C/A;G;T snv 1.6E-04 1.3E-04 40
rs3856806 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 41
rs760043106 0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs1982073 0.649 0.640 19 41353016 missense variant G/A;C snv 32
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs4644 0.732 0.320 14 55138217 missense variant C/A;G snv 0.35 14
rs1801320 0.742 0.160 15 40695330 5 prime UTR variant G/C snv 0.12 15
rs2235544 0.742 0.240 1 53909897 intron variant C/A;T snv 0.53; 4.0E-06 14
rs1453633223 0.807 0.080 9 21974503 missense variant C/T snv 4.0E-06 6
rs660118 0.807 0.080 11 65967703 missense variant G/C snv 0.46 0.36 6
rs745542298 0.807 0.080 1 3732781 missense variant G/A;T snv 8.6E-06; 4.3E-06 2.1E-05 6
rs769809364 0.807 0.080 1 3732940 missense variant G/A snv 8.5E-06 1.4E-05 7