SNTA1
HGNC:11167 · SaudiVarKB evidence summary derived from retained literature mentions.
3Gene mentions
3Publications
0Linked variants
1Associated phenotypes
Associated phenotypes
Co-mentioned in SNTA1 publications| Phenotype | Identifier | Articles | Mentions |
|---|---|---|---|
| Duchenne muscular dystrophy | — | 1 | 1 |
Linked variants
Variants normalized to SNTA1| Variant | HGVS / rsID | Articles | Mentions |
|---|
No normalized variants are linked to this gene.
Population context
Reported in the same publications| Country / region | Group | Cohort | Articles |
|---|---|---|---|
| Not specified | — | 45 | 1 |
| Not specified | — | 979 | 1 |
Supporting publications
3 records- 2024Exploring novel natural compound-based therapies for Duchenne muscular dystrophy management: insights from network pharmacology, QSAR modeling, molecular dynamics, and free energy calculations.Frontiers in pharmacologyPubMed ↗
- 2019Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity.Nature communicationsPubMed ↗
- 2015Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome.PloS onePubMed ↗