PKNOX2, PBX/knotted 1 homeobox 2, 63876

N. diseases: 19; N. variants: 6
Disease: Autosomal dominant compelling helio ophthalmic outburst syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7107770
rs7107770
Entrez Id: 63876
Gene Symbol: PKNOX2
PKNOX2
CUI: C1863416
Disease:
Autosomal dominant compelling helio ophthalmic outburst syndrome 		0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965 2016