rs137852700
A SNP in the PPT1 gene on chromosome 1. Its most notable genotype is A;A: Neuronal Ceroid Lipofuscinosis
- Gene
- PPT1
- Location
- Chr 140,089,495 (GRCh38)
- Highest magnitude
- 5.0Very important
- Tested on
- AncestryDNA
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- G;GGoodcommon in clinvar
- A;GBadNeuronal Ceroid Lipofuscinosis carrier
- A;AMost notableBadNeuronal Ceroid Lipofuscinosis
SNPedia records rs137852700 on the minus strand: (C;C), (C;T), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Notes
From SNPedia
Notes
A;G
Neuronal ceroid lipofuscinosis (PPT1-related)
Source and license
Adapted from rs137852700 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.