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
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs833061 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs3856806 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 41