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rs1799945(G;G)

From SNPedia

Two copies of H63D, likely affected by mild form of hemochromatosis
Is agenotype
ofrs1799945
GeneHFE
Chromosome6
Position26,090,951
Merged fromRs17515604
mentionedby
Magnitude4
ReputeBad
Geno Mag Summary
(C;C) 0 Not a H63D hemochromatosis carrier.
(C;G) 3 One copy of H63D, carrier of hemochromatosis, likely unaffected unless also C282Y carrier.
(G;G) 4 Two copies of H63D, likely affected by mild form of hemochromatosis

You would be expected to experience Hereditary hemochromatosis based on your rs1799945(G;G) H63D status. Without concurrent C282Y rs1800562 (A;G) or (A;A), it is unlikely that you will experience symptoms. This is a treatable condition.