rs149610079
A SNP in the DBR1 gene on chromosome 3. Its most notable genotype is A;G: Carrier of mutation predisposing to brainstem viral encephalitis
- Gene
- DBR1
- Location
- Chr 3138,167,206 (GRCh38)
- Highest magnitude
- 3.0Important
- Tested on
- Not on consumer chips
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;GMost notableBadCarrier of mutation predisposing to brainstem viral encephalitis
- 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.589C>T (p.R197X) Mutation in DBR1 gene pathogenic for predisposition to brainstem viral encephalitis (when inherited recessively);
A;G
Unaffected in absence of a second mutation in the DBR1 gene; see links and discussion via main rs-page.
Source and license
Adapted from rs149610079 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.