rs878855013
A SNP in the ZFYVE26 gene on chromosome 14. Its most notable genotype is -;C: Carrier of a spastic paraplegia type 15 mutation
- Gene
- ZFYVE26
- Location
- Chr 1467,769,731 (GRCh38)
- Highest magnitude
- 3.0Important
- Tested on
- Not on consumer chips
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- -;CMost notableBadCarrier of a spastic paraplegia type 15 mutation
- C;CGoodcommon in clinvar
SNPedia records rs878855013 on the minus strand: (-;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other ZFYVE26 SNPs
- rs118204049A;GCarrier of a spastic paraplegia type 15 mutationImportant
- rs118204050A;GCarrier of a spastic paraplegia type 15 mutationImportant
- rs370828455C;TCarrier of a spastic paraplegia type 15 mutationImportant
- rs370837940G;TCarrier of a spastic paraplegia type 15 mutationImportant
- rs878855011-;GCarrier of a spastic paraplegia type 15 mutationImportant
- rs12891047A;Acommon/normalTypical
Notes
From SNPedia
Notes
aka c.5485-1delG see ZFYVE26
-;C
Unaffected in absence of another ZFYVE26 gene mutation; see ZFYVE26
Source and license
Adapted from rs878855013 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.