rs121918221
A SNP in the SEC23B gene on chromosome 20. Its most notable genotype is A;G: Carrier of a congenital dyserythropoietic anemia type II mutation
- Gene
- SEC23B
- Location
- Chr 2018,515,695 (GRCh38)
- Highest magnitude
- 3.0Important
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- <1%
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;GMost notableBadCarrier of a congenital dyserythropoietic anemia type II 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.
Notes
From SNPedia
Notes
aka c.325G>A (p.Glu109Lys or E109K)
A;G
Unaffected in absence of a second SEC23B gene mutation
Source and license
Adapted from rs121918221 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.