CUX2, cut like homeobox 2, 23316

N. diseases: 87; N. variants: 21
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3847953
rs3847953
Entrez Id: 23316
Gene Symbol: CUX2
CUX2
CUI: C0005586
Disease:
Bipolar Disorder
0.010 GeneticVariation BEFREE Two SNPs (rs3847953 and rs933399) and an insertion/deletion with putative functional relevance (which are in high LD with each other and with the microsatellite marker) showed significant or nearly significant association with bipolar disorder after Bonferroni-correction (reaching nominal P values from P = 0.002 to P = 0.005). 15389760 2005