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 0.030 1.000 3 2006 2016
dbSNP: rs1800562
rs1800562
HFE ; LOC108783645
262 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.020 1.000 2 2003 2012
dbSNP: rs104893664
rs104893664
SLC40A1
2 0.925 0.080 2 189564186 missense variant C/T snv 4.4E-05 0.010 1.000 1 2005 2005
dbSNP: rs104893673
rs104893673
SLC40A1
2 0.925 0.080 2 189575193 missense variant C/A snv 0.010 1.000 1 2005 2005