rs17329669
A SNP on chromosome 7. Its most notable genotype is A;A.
- Gene
- None listed
- Location
- Chr 736,812,324 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, FamilyTreeDNA
- Minor allele frequency
- 8%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (A;A). 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.
- AverageA;A 89%
- European ancestry (Utah)A;A 65%
- Han Chinese (Beijing)A;A 100%
- Japanese (Tokyo)A;A 100%
- Yoruba (Nigeria)A;A 91%
Notes
From SNPedia
Notes
rs17329669 is an intergenic SNP on chromosome 7 between the AOAH gene and the ELMO1 gene (genes involved in neutrophils / possibly immune related). rs17329669 (G) was associated with Parkinson's disease in a discordant sibling study No evidence for association with Parkinson disease for 13 single-nucleotide polymorphisms identified by whole-genome association screening. A case-control association study of the 12 single-nucleotide polymorphisms implicated in Parkinson disease by a recent genome scan.
Source and license
Adapted from rs17329669 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.