rs121917967(A;T)
Dravet syndrome and severe epileptic seizure syndrome(s) possible
- Magnitude
- 8.0Very important
- Repute
- Bad
- On SNPedia
- rs121917967(A;T)Minus strand
- Gene
- SCN1A
Other genotypes of rs121917967
Notes
From SNPedia
Originally classified as a variant of unknown significance (VUS); more recently considered likely to be pathogenic. See discussion at rs121917967.
Related
Source and license
Adapted from rs121917967(A;T) 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.