rs53576, OXTR;CAV3

N. diseases: 42
Disease: Prosopagnosia ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Prosopagnosia
CUI: C0234512
Disease: Prosopagnosia
0.010 GeneticVariation BEFREE We found evidence of an association between the common genetic variants rs53576 and rs2254298 OXTR SNPs and prosopagnosia. 27693815 2016