Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs2071303
LOC108783645 ; HFE
0.882 0.120 6 26091108 splice region variant T/C snv 0.38 0.36 3
rs1572982
HFE
0.827 0.200 6 26094139 intron variant G/A;T snv 0.52; 8.0E-06 2
rs6918586
HFE
0.882 0.160 6 26097156 3 prime UTR variant T/C snv 0.45 2