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rs1799990(A;G)

From SNPedia

Resistance 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 population
Is agenotype
ofrs1799990
GenePRNP
Chromosome20
Position4,699,605
mentionedby
Magnitude2.1
ReputeGood
Geno Mag Summary
(A;A) 2.3 Increased chance of Prion Disease (PrP 129 Met homozygote)
(A;G) 2.1 Resistance 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 population
(G;G) 2 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

This genotype codes for Met/Val heterozygote at codon 129 in PrP, the Prion Protein. This is strongly protective against development of sporadic, 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 [PMID 23399523]

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]