rs796053361
A SNP in the STXBP1 gene on chromosome 9. Its most notable genotype is A;G: Early infantile epileptic encephalopathy, type 4
- Gene
- STXBP1
- Location
- Chr 9127,668,160 (GRCh38)
- Highest magnitude
- 8.0Very important
- Tested on
- 23andMe, AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;GMost notableBadEarly infantile epileptic encephalopathy, type 4
- 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 STXBP1 SNPs
- rs121918317A;GEarly infantile epileptic encephalopathy, type 4Very important
- rs121918318A;GEarly infantile epileptic encephalopathy, type 4Very important
- rs121918319G;TEarly infantile epileptic encephalopathy, type 4Very important
- rs121918320A;TEarly infantile epileptic encephalopathy, type 4Very important
- rs121918321C;TEarly infantile epileptic encephalopathy, type 4Very important
- rs587776641A;GEarly infantile epileptic encephalopathy, type 4Very important
- rs587777310A;GEarly infantile epileptic encephalopathy, type 4Very important
- rs587784454-;ATEarly infantile epileptic encephalopathy, type 4Very important
Notes
From SNPedia
Notes
A;G
see discussion at STXBP1
Source and license
Adapted from rs796053361 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.