PRRX2, paired related homeobox 2, 51450

N. diseases: 46; N. variants: 1
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7866070
rs7866070
Entrez Id: 51450
Gene Symbol: PRRX2
PRRX2
CUI: C0004106
Disease:
Astigmatism 		0.700 GeneticVariation GWASCAT Web-based, participant-driven studies yield novel genetic associations for common traits. 20585627 2010