SYNPO
HGNC:30672 · SaudiVarKB evidence summary derived from retained literature mentions.
1Gene mentions
1Publications
0Linked variants
2Associated phenotypes
Associated phenotypes
Co-mentioned in SYNPO publications| Phenotype | Identifier | Articles | Mentions |
|---|---|---|---|
| renal failure | — | 1 | 1 |
| nephrotic syndrome | — | 1 | 1 |
Linked variants
Variants normalized to SYNPO| 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 | — | 1,382 | 1 |
Supporting publications
1 records- 2021Generation of Monogenic Candidate Genes for Human Nephrotic Syndrome Using 3 Independent Approaches.Kidney international reportsPubMed ↗