rs80358229
A SNP in the SLC2A10 gene on chromosome 20. Its most notable genotype is A;G: Carrier of an arterial tortuosity syndrome mutation
- Gene
- SLC2A10
- Location
- Chr 2046,725,546 (GRCh38)
- Highest magnitude
- 3.0Important
- Tested on
- AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;GMost notableBadCarrier of an arterial tortuosity syndrome mutation
- G;GGoodcommon in clinvar
On SNPedia: (A;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other SLC2A10 SNPs
- rs121908172G;TCarrier of an arterial tortuosity syndrome mutationImportant
- rs370547023C;TCarrier of an arterial tortuosity syndrome mutationImportant
- rs564317065A;GCarrier of an arterial tortuosity syndrome mutationImportant
- rs572620317A;TCarrier of an arterial tortuosity syndrome mutationImportant
- rs587776599-;GCarrier of an arterial tortuosity syndrome mutationImportant
- rs587776600-;GCarrier of an arterial tortuosity syndrome mutationImportant
- rs763220502A;GCarrier of an arterial tortuosity syndrome mutationImportant
- rs864309478A;CCarrier of an arterial tortuosity syndrome mutationImportant
Notes
From SNPedia
Notes
A;G
Likely to be unaffected in absence of a second SLC2A10 gene mutation
Source and license
Adapted from rs80358229 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.