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
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs3745274 0.672 0.480 19 41006936 missense variant G/A;T snv 4.0E-06; 0.27 30
rs121918464 0.708 0.440 12 112450406 missense variant G/A;C snv 25
rs562015640 0.742 0.360 10 87960957 stop gained A/G;T snv 1.2E-05 16
rs1239681664 0.716 0.320 9 104818690 synonymous variant A/G snv 7.0E-06 15
rs559063155 0.732 0.280 2 197402110 stop gained T/A;C;G snv 9.0E-05 14
rs2239633 0.742 0.240 14 23119848 upstream gene variant G/A snv 0.38 12
rs35201683
HFE
0.732 0.360 6 26094205 stop gained C/A;T snv 1.4E-03 12
rs780246573 0.732 0.360 6 26092860 stop gained C/G;T snv 4.0E-06; 8.0E-06 12
rs80338880 0.732 0.360 7 100633100 stop gained G/C snv 7.0E-06 12
rs1470755915 0.776 0.240 8 92005229 missense variant C/A snv 7.0E-06 10
rs927698341 0.776 0.240 8 92005280 synonymous variant C/A snv 4.0E-06 2.8E-05 10
rs11978267 0.763 0.240 7 50398606 intron variant A/G snv 0.25 9
rs111033563 0.776 0.240 6 26092916 missense variant A/C snv 4.0E-06 8
rs797045145 0.807 0.240 6 26091479 stop gained G/A snv 6
rs1057519766 0.851 0.080 13 28028203 missense variant G/C;T snv 5