rs1799990(G;G)

Resistance to vCJD (PrP 129 Val homozygous), 1.7x reduced risk of sporadic CJD and 0.87x reduced risk for late-onset Alzheimer in a Caucasian population

Magnitude
2.0Worth knowing
Repute
Good
Frequency
9%Average of 11 populations
On SNPedia
rs1799990(G;G)
Gene
PRNP

Frequency

Share of people with G;G in each HapMap population.

  • African ancestry (Southwest US)19%
  • Maasai (Kenya)19%
  • Mexican ancestry (Los Angeles)16%
  • Tuscan15%
  • European ancestry (Utah)13%
  • Yoruba (Nigeria)10%
  • Luhya (Kenya)6%
  • Gujarati Indian5%
  • Han Chinese (Beijing)<1%
  • Japanese (Tokyo)0%
  • Chinese (Denver)0%

Other genotypes of rs1799990

  1. A;AMost notableBadIncreased chance of Prion Disease (PrP 129 Met homozygote)Worth knowing · 2.358% of people
  2. A;GGoodResistance to vCJD (PrP 129 Met/Val heterozygote), 4.6x reduced risk of sporadic CJD and 0.87x reduced risk for late-onset Alzheimer in a Caucasian populationWorth knowing · 2.132% of people

All about rs1799990

Notes

From SNPedia

This genotype codes for Val/Val homozygous at codon 129 in PrP, the Prion Protein. This is slightly protective against development of sporadic CJD, and confers resistance against vCJD. Studies in Papua New Guinea showed that this genotype prevents transmission of kuru PMID 19923577, a form of Prion disease transmitted by cannibalism. So eat as many brains as you want! A total of 4228 cases and 4324 controls in 16 case-control studies were included in the meta-analysis. The results indicated that the variant V allele carriers (VV+MV) had a 13% decreased risk of AD, when compared with the homozygote MM A 2006 study compared 593 Germans with sporadic CJD (sCJD) to 748 healthy controls. The researchers found an unusual pattern - people with one copy of each variant at rs1799990, a SNP in the gene PRNP, were less likely to have sCJD compared to those who had two identical copies of either the A or G type. People with the AG genotype had 4.6 times lower odds of sCJD compared to those with AA; a G at both copies of the SNP reduced a subject's odds of having sCJD 1.7 times.PMID 17047093 All reported cases of vCJD, (linked to ingestion of 'mad cow disease' contaminated meat) have been 129 Met homozygous PMID 22505363

Source and license

Adapted from rs1799990(G;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.