rs9851967

A SNP in the LPP gene on chromosome 3. Its most notable genotype is C;C: normal

Gene
LPP
Location
Chr 3188,369,840 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
32%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;CMost notableNot ratednormalTypical · 0.056% of people
  2. C;TGood0.88x risk of vitiligo in ChineseTypical · 0.035% of people
  3. T;TGood0.88x risk of vitiligo in ChineseTypical · 0.09% of people

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

Frequency

Share of each genotype in 11 HapMap populations.

  • AverageC;C 56% C;T 35% T;T 9%
  • European ancestry (Utah)C;C 26% C;T 57% T;T 18%
  • Han Chinese (Beijing)C;C 43% C;T 47% T;T 10%
  • Japanese (Tokyo)C;C 45% C;T 40% T;T 15%
  • Yoruba (Nigeria)C;C 91% C;T 9% T;T 0%
  • African ancestry (Southwest US)C;C 79% C;T 19% T;T 2%
  • Chinese (Denver)C;C 59% C;T 35% T;T 6%
  • Gujarati IndianC;C 59% C;T 35% T;T 6%
  • Luhya (Kenya)C;C 80% C;T 20% T;T 0%
  • Mexican ancestry (Los Angeles)C;C 46% C;T 45% T;T 9%
  • Maasai (Kenya)C;C 65% C;T 30% T;T 5%
  • TuscanC;C 25% C;T 49% T;T 27%

Conditions, medicines and genes

Other LPP SNPs

All LPP SNPs

Notes

From SNPedia

Notes

Celiac Disease

Source and license

Adapted from rs9851967 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.