rs370828455
A SNP in the ZFYVE26 gene on chromosome 14. Its most notable genotype is C;T: Carrier of a spastic paraplegia type 15 mutation
- Gene
- ZFYVE26
- Location
- Chr 1467,782,971 (GRCh38)
- Highest magnitude
- 3.0Important
- Tested on
- 23andMe, AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;CGoodcommon in clinvar
- C;TMost notableBadCarrier of a spastic paraplegia type 15 mutation
On SNPedia: (C;C), (C;T). 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
- rs370837940G;TCarrier of a spastic paraplegia type 15 mutationImportant
- rs878855011-;GCarrier of a spastic paraplegia type 15 mutationImportant
- rs878855013-;CCarrier of a spastic paraplegia type 15 mutationImportant
- rs12891047A;Acommon/normalTypical
Notes
From SNPedia
Notes
aka c.4181G>A, p.Trp1394Ter and W1394X see ZFYVE26
C;T
Unaffected in absence of another ZFYVE26 gene mutation; see ZFYVE26
Source and license
Adapted from rs370828455 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.