Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs1801278 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 38
rs1045485 0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 34
rs1042821 0.732 0.280 2 47783349 missense variant G/A;C;T snv 0.18; 8.6E-06 16
rs536562413 0.732 0.240 2 47799934 missense variant A/G snv 1.2E-05 7.0E-06 15
rs63750875 0.742 0.280 2 47475171 missense variant G/A;C snv 1.6E-05 15
rs4987188 0.790 0.200 2 47416318 missense variant G/A;T snv 1.3E-02; 2.0E-05 11
rs16840252 0.776 0.480 2 203866796 upstream gene variant C/T snv 0.16 8
rs2302615 0.807 0.120 2 10448012 intron variant C/T snv 0.31 7
rs910532454 0.882 0.080 2 136115453 missense variant C/A;T snv 4.0E-06 4
rs147198552 0.882 0.080 2 136115450 missense variant C/T snv 1.2E-05 7.0E-06 3
rs2059691 0.882 0.080 2 178437157 intron variant A/G snv 0.72 3
rs1724120 0.925 0.080 2 96143592 3 prime UTR variant T/C snv 0.53 2
rs1967327 0.925 0.080 2 178449632 intron variant G/A;C;T snv 2
rs587780669 0.925 0.080 2 47798999 missense variant C/A;G;T snv 2
rs730881756 0.925 0.080 2 47445653 missense variant A/C;G snv 4.0E-06 2
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
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
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 44
rs1801725 0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 39
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs187084 0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30