rs35095275

A SNP in the GBAP1 gene on chromosome 1. Its most notable genotype is A;A: risk allele, but prone to genotyping confusion

Gene
GBAP1
Location
Chr 1155,205,043 (GRCh38)
Highest magnitude
6.0Very important
Tested on
Not on consumer chips

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;AMost notableBadrisk allele, but prone to genotyping confusionVery important · 6.0
  2. A;GNot ratedcarrier for parkinson's risk?Important · 3.0
  3. G;GNot ratedmost common; unaffectedTypical · 0.0

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

Other GBAP1 SNPs

All GBAP1 SNPs

Notes

From SNPedia

Notes

Note: this SNP has been retired and replaced by rs421016, representing the exact same nucleotide position yet on the other strand, possibly with more specific flanking sequence.

A;A

See rs421016(T;T) and rs421016. This position has been linked to increased risk of Parkinson Disease but was also a changed significantly between build 36 and 37 of the reference human genome. If detected please inform info@snpedia.com with details about how your genotyping was performed and analyzed.

A;G

This position has been renamed between build 36 and 37 of the reference human genome. This genotype seems to indicate some additional risk, so please see rs421016 for more information.

Source and license

Adapted from rs35095275 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.