rs150938052
A SNP in the SYCE2 gene on chromosome 19. Its most notable genotype is C;T: Carrier of a Glutaric aciduria type I mutation
- Gene
- SYCE2
- Location
- Chr 1912,897,767 (GRCh38)
- Highest magnitude
- 3.0Important
- Tested on
- AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;CGoodcommon in clinvar
- C;TMost notableBadCarrier of a Glutaric aciduria type I 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 SYCE2 SNPs
- rs121434369T;Tglutaric acidemia type IVery important
- rs141437721A;GCarrier of a Glutaric aciduria type I mutationImportant
- rs147611168A;GCarrier of a Glutaric aciduria type I mutationImportant
- rs372983141C;GCarrier of a Glutaric aciduria type I mutationImportant
- rs752127949C;TCarrier of a Glutaric aciduria type I mutationImportant
Notes
From SNPedia
Notes
C;T
Unaffected in absence of a second GCDH gene mutation; see text and links via main rs-page
Source and license
Adapted from rs150938052 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.