SETD4, SET domain containing 4, 54093

N. diseases: 15; N. variants: 5
Disease: Complete Trisomy 21 Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs9024
rs9024
Entrez Id: 873;54093;100133286
Gene Symbol: CBR1;SETD4;LOC100133286
CBR1;SETD4;LOC100133286
CUI: C4521042
Disease:
Complete Trisomy 21 Syndrome 		0.010 GeneticVariation BEFREE CBR1 rs9024 genotype status impacts on cardiac CBR1 expression in non-DS hearts. 24562808 2014