Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11978267 0.763 0.240 7 50398606 intron variant A/G snv 0.25 7
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs562015640 0.742 0.360 10 87960957 stop gained A/G;T snv 1.2E-05 15
rs387906659 0.742 0.280 19 40257052 stop gained C/A;T snv 13
rs559063155 0.732 0.280 2 197402110 stop gained T/A;C;G snv 9.0E-05 13
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
rs797045145 0.807 0.240 6 26091479 stop gained G/A snv 5
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
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 264
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 230
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 221
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 201
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 181
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 169
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 114
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 92
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77