CRYAA
HGNC:2388 · SaudiVarKB evidence summary derived from retained literature mentions.
2Gene mentions
2Publications
4Linked variants
1Associated phenotypes
Associated phenotypes
Co-mentioned in CRYAA publications| Phenotype | Identifier | Articles | Mentions |
|---|---|---|---|
| congenital cataract | — | 2 | 2 |
Linked variants
Variants normalized to CRYAA| Variant | HGVS / rsID | Articles | Mentions |
|---|---|---|---|
| rs13053109 | rs13053109 | 1 | 1 |
| rs3761382 | rs3761382 | 1 | 1 |
| rs7278468 | rs7278468 | 1 | 1 |
| rs13051039 | rs13051039 | 1 | 1 |
Population context
Reported in the same publications| Country / region | Group | Cohort | Articles |
|---|---|---|---|
| Not specified | — | 196 | 1 |
| Saudi Arabia | — | 26 | 1 |
Supporting publications
2 records- 2022Association of single nucleotide polymorphism variations in CRYAA and CRYAB genes with congenital cataract in Pakistani population.Saudi journal of biological sciencesPubMed ↗
- 2015Phenotypes of Recessive Pediatric Cataract in a Cohort of Children with Identified Homozygous Gene Mutations (An American Ophthalmological Society Thesis).Transactions of the American Ophthalmological SocietyPubMed ↗