Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1800730
HFE ; LOC108783645
0.649 0.480 6 26090957 missense variant A/T snv 1.0E-02 1.0E-02 32
rs35201683
HFE
0.732 0.360 6 26094205 stop gained C/A;T snv 1.4E-03 12
rs780246573
HFE ; LOC108783645
0.732 0.360 6 26092860 stop gained C/G;T snv 4.0E-06; 8.0E-06 12
rs111033563
LOC108783645 ; HFE
0.776 0.240 6 26092916 missense variant A/C snv 4.0E-06 8
rs1572982
HFE
0.827 0.200 6 26094139 intron variant G/A;T snv 0.52; 8.0E-06 7
rs707889
HFE
0.827 0.200 6 26095703 3 prime UTR variant G/A;T snv 6
rs765545512
HFE
0.827 0.240 6 26093226 missense variant G/A;T snv 4.0E-06; 1.6E-05 6
rs797045145
HFE ; LOC108783645
0.807 0.240 6 26091479 stop gained G/A snv 6
rs2071303
LOC108783645 ; HFE
0.882 0.120 6 26091108 splice region variant T/C snv 0.38 0.36 6
rs79220007
HFE
6 26098246 3 prime UTR variant T/C snv 3.8E-02 5
rs1167115018
HFE ; LOC108783645
0.827 0.160 6 26092760 missense variant A/G snv 8.0E-06 7.0E-06 5
rs143175221
LOC108783645 ; HFE
0.827 0.200 6 26092952 missense variant T/C snv 8.4E-04 5.6E-04 5
rs2794719
LOC108783645 ; HFE
0.925 0.120 6 26088662 intron variant T/C;G snv 5
rs2006736
HFE ; LOC108783645
0.925 0.120 6 26085789 upstream gene variant C/G;T snv 4
rs1800702
LOC108783645 ; HFE
0.925 0.120 6 26086235 upstream gene variant C/G snv 0.37 4
rs2794720
LOC108783645 ; HFE
0.925 0.120 6 26086974 upstream gene variant G/C snv 0.37 4
rs12346
HFE
0.925 0.120 6 26096818 3 prime UTR variant T/C snv 0.76 3
rs6918586
HFE
0.882 0.160 6 26097156 3 prime UTR variant T/C snv 0.45 3
rs755284374
HFE
0.882 0.120 6 26093122 missense variant C/A;T snv 4.0E-06; 4.0E-06 3
rs897206619
HFE
0.882 0.120 6 26093128 missense variant C/T snv 3.5E-05 3
rs1431315635
HFE ; LOC108783645
0.882 0.120 6 26092928 missense variant C/T snv 4.0E-06 3
rs781516027
LOC108783645 ; HFE
0.882 0.080 6 26092744 missense variant C/G;T snv 8.0E-06; 3.6E-05 3
rs2858996
HFE
0.925 0.080 6 26093798 intron variant G/A;C;T snv 2