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
226 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.800 1.000 3 2012 2018
dbSNP: rs1800562
rs1800562
262 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.700 1.000 2 2010 2012
dbSNP: rs12346
rs12346
HFE
3 0.925 0.120 6 26096818 3 prime UTR variant T/C snv 0.76 0.700 1.000 1 2012 2012
dbSNP: rs1800702
rs1800702
4 0.925 0.120 6 26086235 upstream gene variant C/G snv 0.37 0.700 1.000 1 2012 2012
dbSNP: rs2006736
rs2006736
4 0.925 0.120 6 26085789 upstream gene variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs2071303
rs2071303
6 0.882 0.120 6 26091108 splice region variant T/C snv 0.38 0.36 0.700 1.000 1 2012 2012
dbSNP: rs2794719
rs2794719
5 0.925 0.120 6 26088662 intron variant T/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs2794720
rs2794720
4 0.925 0.120 6 26086974 upstream gene variant G/C snv 0.37 0.700 1.000 1 2012 2012
dbSNP: rs707889
rs707889
HFE
6 0.827 0.200 6 26095703 3 prime UTR variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs79220007
rs79220007
HFE
5 6 26098246 3 prime UTR variant T/C snv 3.8E-02 0.700 1.000 1 2016 2016