ITGA2
HGNC:6137 · SaudiVarKB evidence summary derived from retained literature mentions.
2Gene mentions
2Publications
0Linked variants
1Associated phenotypes
Associated phenotypes
Co-mentioned in ITGA2 publications| Phenotype | Identifier | Articles | Mentions |
|---|---|---|---|
| sickle cell disease | HP:0001878 | 1 | 1 |
Linked variants
Variants normalized to ITGA2| 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 | — | 72 | 1 |
| Not specified | — | 100 | 1 |
Supporting publications
2 records- 2020L-Selectin P213S and Integrin Alpha 2 C807T Genetic Polymorphisms in Pediatric Sickle Cell Disease Patients.Journal of pediatric hematology/oncologyPubMed ↗
- 2019Molecular yield of targeted sequencing for Glanzmann thrombasthenia patients.NPJ genomic medicinePubMed ↗