rs3130352

A SNP in the UBQLN1P gene on chromosome 6. Its most notable genotype is C;C: common on affy axiom data

Gene
UBQLN1P
Location
Chr 630,360,580 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, FamilyTreeDNA
Minor allele frequency
4%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;CMost notableGoodcommon on affy axiom dataTypical · 0.093% of people

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

Frequency

Share of each genotype in 9 HapMap populations.

  • AverageC;C 93%
  • European ancestry (Utah)C;C 79%
  • Han Chinese (Beijing)C;C 100%
  • Japanese (Tokyo)C;C 100%
  • Yoruba (Nigeria)C;C 96%
  • African ancestry (Southwest US)C;C 93%
  • Luhya (Kenya)C;C 89%
  • Mexican ancestry (Los Angeles)C;C 97%
  • Maasai (Kenya)C;C 98%
  • TuscanC;C 89%

Conditions, medicines and genes

Notes

From SNPedia

Notes

HLA-DQB1 8.1 haplotype is associated with significantly lower risk for type-1 diabetes *rs2157678(T) *rs3130380(A) *rs3094628(C) *rs3130352(T)

Source and license

Adapted from rs3130352 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.