rs1057519290
A SNP in the ATP13A2 gene on chromosome 1. Its most notable genotype is -;-: Spastic paraplegia, type 78
- Gene
- ATP13A2
- Location
- Chr 116,986,886 (GRCh38)
- Highest magnitude
- 7.8Very important
- Tested on
- Not on consumer chips
Genotypes
As shown in 23andMe and AncestryDNA files.
- -;-Most notableBadSpastic paraplegia, type 78
- -;TCTBadCarrier of a spastic paraplegia mutation (type 78)
- TCT;TCTGoodcommon/normal
On SNPedia: (-;-), (-;TCT), (TCT;TCT). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other ATP13A2 SNPs
- rs121918227G;GParkinson's mutation, type 9, early-onsetVery important
- rs144701072T;TParkinson's mutation, type 9, early-onsetVery important
- rs199624796A;AParkinson's mutation, type 9, early-onsetVery important
- rs587776890-;-Parkinson's mutation, type 9, early-onsetVery important
- rs587777053G;GParkinson's mutation, type 9, early-onsetVery important
- rs749798211-;-Parkinson's mutation, type 9, early-onsetVery important
- rs762033589TC;TCParkinson's mutation, type 9, early-onsetVery important
- rs786205056T;TParkinson's mutation, type 9, early-onsetVery important
Notes
From SNPedia
Notes
c.3152_3154delTCT (p.Phe1051del)
-;-
see ATP13A2
-;TCT
see ATP13A2
Source and license
Adapted from rs1057519290 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.