rs1800206

A SNP in the PPARA gene on chromosome 22. Its most notable genotype is C;C: common in complete genomics

Gene
PPARA
Location
Chr 2246,218,377 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
2%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;CMost notableGoodcommon in complete genomicsTypical · 0.098% of people
  2. C;GNot ratedNo summary available.Typical · 0.02% of people

On SNPedia: (C;C), (C;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Frequency

Share of each genotype in 4 HapMap populations.

  • AverageC;C 98% C;G 2%
  • European ancestry (Utah)C;C 92% C;G 8%
  • Han Chinese (Beijing)C;C 100% C;G 0%
  • Japanese (Tokyo)C;C 100% C;G 0%
  • Yoruba (Nigeria)C;C 100% C;G 0%

Other PPARA SNPs

All PPARA SNPs

Source and license

Adapted from rs1800206 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.