rs86312

A SNP in the NAGLU gene on chromosome 17. Its most notable genotype is C;C: common in clinvar

Gene
NAGLU
Location
Chr 1742,544,215 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
12%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;CMost notableGoodcommon in clinvarTypical · 0.05% of people
  2. G;GGoodcommon genotypeTypical · 0.082% of people

On SNPedia: (C;C), (G;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 5% G;G 82%
  • European ancestry (Utah)C;C 0% G;G 92%
  • Han Chinese (Beijing)C;C 0% G;G 98%
  • Japanese (Tokyo)C;C 0% G;G 100%
  • Yoruba (Nigeria)C;C 19% G;G 40%

Other NAGLU SNPs

All NAGLU SNPs

Source and license

Adapted from rs86312 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.