rs1799945(G;G)

Two copies of H63D, likely affected by mild form of hemochromatosis

Magnitude
4.0Very important
Repute
Bad
Frequency
0%Average of 4 populations
On SNPedia
rs1799945(G;G)
Gene
LOC108783645

Frequency

Share of people with G;G in each HapMap population.

  • European ancestry (Utah)0%
  • Han Chinese (Beijing)0%
  • Japanese (Tokyo)0%
  • Yoruba (Nigeria)0%

Other genotypes of rs1799945

  1. C;CGoodNot a H63D hemochromatosis carrier.Typical · 0.083% of people
  2. C;GBadOne copy of H63D, carrier of hemochromatosis, likely unaffected unless also C282Y carrier.Important · 3.017% of people

All about rs1799945

Notes

From SNPedia

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.

Source and license

Adapted from rs1799945(G;G) on SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.

SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.