SCNN1G
HGNC:10602 · SaudiVarKB evidence summary derived from retained literature mentions.
2Gene mentions
2Publications
0Linked variants
1Associated phenotypes
Associated phenotypes
Co-mentioned in SCNN1G publications| Phenotype | Identifier | Articles | Mentions |
|---|---|---|---|
| hypertension | — | 1 | 1 |
Linked variants
Variants normalized to SCNN1G| 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 |
|---|---|---|---|
| Saudi Arabia | — | 22 | 1 |
Supporting publications
2 records- 2021A Unique Genotype of Pseudohypoaldosteronism Type 1b in a Highly Consanguineous Population.Journal of the Endocrine SocietyPubMed ↗
- 2021A Rare Case of Familiar Hypertension Presenting with Hypertensive Encephalopathy in an Elderly Patient: A Diagnostic Dilemma: A Presentation of Liddle's Syndrome due to Novel Mutation in SCNN1G Gene.Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi ArabiaPubMed ↗