Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28834970
rs28834970
PTK2B
CUI: C1842937
Disease: AURAL ATRESIA, CONGENITAL
AURAL ATRESIA, CONGENITAL 		0.010 GeneticVariation BEFREE We observed significant associations of CAA pathology with APOEɛ4 and PTK2B rs28834970. 31256143

2019