Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1799945
rs1799945
HFE ; LOC108783645
226 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1.000 1 2008 2008
dbSNP: rs1801198
rs1801198
TCN2
26 0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 0.010 1.000 1 2006 2006
dbSNP: rs3760776
rs3760776
FUT6
3 0.925 0.120 19 5839735 upstream gene variant G/A snv 0.22 0.010 1.000 1 2015 2015
dbSNP: rs9606756
rs9606756
TCN2
7 0.790 0.160 22 30610873 missense variant A/G snv 0.12 0.14 0.010 1.000 1 2015 2015