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
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs1061622 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33
rs8193037 0.752 0.320 6 52186311 upstream gene variant G/A;T snv 12