rs869312029
A SNP in the SLC25A38 gene on chromosome 3. Its most notable genotype is A;G: carrier of one allele for a sideroblastic anemia disorder
- Gene
- SLC25A38
- Location
- Chr 339,391,440 (GRCh38)
- Highest magnitude
- 3.0Important
- Tested on
- AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;GMost notableBadcarrier of one allele for a sideroblastic anemia disorder
- G;GGoodcommon/normal
On SNPedia: (A;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Notes
From SNPedia
Notes
aka c.277-1G>A reported in ClinVar as pathogenic for anemia, sideroblastic, pyridoxine-refractory (an autosomal recessive condition)
A;G
see rs869312029
Source and license
Adapted from rs869312029 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.