Source: GWASCAT

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 18
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 16
rs79220007
HFE
6 26098246 3 prime UTR variant T/C snv 3.8E-02 5
rs61472021
HFE ; LOC108783645
1.000 0.040 6 26089797 intron variant T/C snv 0.17 2
rs2032451
LOC108783645 ; HFE
6 26091942 intron variant G/T snv 0.10 2
rs1572982
HFE
0.827 0.200 6 26094139 intron variant G/A;T snv 0.52; 8.0E-06 1
rs6918586
HFE
0.882 0.160 6 26097156 3 prime UTR variant T/C snv 0.45 1
rs56275179
HFE ; LOC108783645
1.000 0.040 6 26089112 intron variant G/C;T snv 1
rs2071303
LOC108783645 ; HFE
0.882 0.120 6 26091108 splice region variant T/C snv 0.38 0.36 1