ITGA2B, integrin subunit alpha 2b, 3674

N. diseases: 215; N. variants: 36
Disease: Glanzmann Thrombasthenia, Autosomal Dominant ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs766503255
rs766503255
Entrez Id: 3674
Gene Symbol: ITGA2B
ITGA2B
CUI: C1861195
Disease:
Glanzmann Thrombasthenia, Autosomal Dominant 		0.800 GeneticVariation UNIPROT
dbSNP: rs766503255
rs766503255
Entrez Id: 3674
Gene Symbol: ITGA2B
ITGA2B
CUI: C1861195
Disease:
Glanzmann Thrombasthenia, Autosomal Dominant 		A 0.800 CausalMutation CLINVAR