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: rs1800562
rs1800562
262 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.800 1.000 3 2010 2018
dbSNP: rs79220007
rs79220007
HFE
5 6 26098246 3 prime UTR variant T/C snv 3.8E-02 0.700 1.000 1 2019 2019