rs1800435(C;G)
Carrier of an ALAD deficiency porphyria mutation
- Magnitude
- 3.0Important
- Repute
- Bad
- Frequency
- 0%Average of 1 populations
- On SNPedia
- rs1800435(C;G)Minus strand
- Gene
- ALAD
Frequency
Share of people with C;G in each HapMap population.
- Yoruba (Nigeria)0%
Other genotypes of rs1800435
Notes
From SNPedia
Unaffected in absence of a second mutation in the ALAD gene; see links via main rs-page and the ALAD gene page
Source and license
Adapted from rs1800435(C;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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.