Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1801198
TCN2
0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 26
rs9606756
TCN2
0.790 0.160 22 30610873 missense variant A/G snv 0.12 0.14 7
rs3760776
FUT6
0.925 0.120 19 5839735 upstream gene variant G/A snv 0.22 3